Section DHS 157.76 - Fluoroscopic equipment Only image-intensified or direct-digital receptor fluoroscopic equipment shall be used for fluoroscopy. Equipment for fluoroscopic imaging or for recording images from the fluoroscopic image receptor, except computed tomography x-ray systems manufactured on or after November 29, 1984, shall meet all the following requirements:
(1) LIMITATION OF USEFUL BEAM. (a) The fluoroscopic imaging assembly shall be provided with a primary protective barrier which intercepts the entire cross section of the useful beam at any source to image distance. The x-ray tube used for fluoroscopy shall not produce x-rays unless the barrier is in position to intercept the entire useful beam. The air kerma rate due to transmission through the barrier with the attenuation block in the useful beam combined with radiation from the fluoroscopic image receptor shall not exceed 3.34 x 10 -3 percent of the entrance air kerma rate, at a distance of 10 cm from any accessible surface of the fluoroscopic imaging assembly beyond the plane of the image receptor.(b) Compliance shall be determined as follows: 1. The air kerma rate shall be measured as required under sub. (4). The air kerma rate due to transmission through the primary barrier combined with radiation from the fluoroscopic image receptor shall be determined by measurements averaged over an area of 100 square cm with no linear dimension greater than 20 cm.2. If the source is below the tabletop, the measurement shall be made with the input surface of the fluoroscopic imaging assembly positioned 30 cm above the tabletop. If the source is above the tabletop and the source to image distance is variable, the measurement shall be made with the end of the beam-limiting device or spacer as close to the tabletop as it can be placed, provided that it shall not be closer than 30 cm.3. Movable grids and compression devices shall be removed from the useful beam during the measurement.4. For all measurements, the attenuation block shall be positioned in the useful beam 10 cm from the point of measurement of entrance air kerma rate and between this point and the input surface of the fluoroscopic imaging assembly.(c) Radiation therapy simulation systems shall be exempt from this requirement provided the systems are intended only for remote control operation and the manufacturer sets forth instructions for assemblers with respect to control location as part of the information required in 21 CFR 1020.30(g).(2) FIELD LIMITATION. (a) For fluoroscopic equipment manufactured after February 25, 1978, when the angle between the image receptor and the beam axis of the x-ray beam is variable, means shall be provided to indicate when the axis of the x-ray beam is perpendicular to the plane of the image receptor. Compliance with par. (e) 1. and 2. shall be determined with the beam axis indicated to be perpendicular to the plane of the image receptor.(b) Means shall be provided to permit further limitation of the x-ray field to sizes smaller than the limits of par. (e) 1. and 2. Beam limiting devices manufactured after May 22, 1979, and incorporated in equipment with a variable source to image distance, the capability of a visible area of greater than 300 square cm, or both, shall be provided with means for stepless adjustment of the x-ray field. Equipment with a fixed source to image distance and the capability of a visible area of no greater than 300 square cm shall be provided with either stepless adjustment of the x-ray field or with a means to further limit the x-ray field size at the plane of the image receptor to 125 square cm or less. Stepless adjustment shall, at the greatest source to image distance, provide continuous field sizes from the maximum obtainable to a field size containable in a square of 5 cm by 5 cm. This paragraph does not apply to intensified fluoroscopy units without image intensification.(c) The x-ray field produced by non-image-intensified fluoroscopic equipment shall not extend beyond the entire visible area of the image receptor. Means shall be provided for stepless adjustment of field size. The minimum field size, at the greatest source to image distance, shall be containable in a square of 5 cm by 5 cm.(d) For fluoroscopic equipment with inherently circular image receptors manufactured before June 10, 2006, other than radiation therapy simulation systems, all the following applies: 1. Neither the length nor the width of the x-ray field in the plane of the image receptor shall exceed that of the visible area of the image receptor by more than 3% of the source to image distance. The sum of the excess length and the excess width shall be no greater than 4% of the source to image distance.2. For rectangular x-ray fields used with circular image receptors, the error in alignment shall be determined along the length and width dimensions of the x-ray field which pass through the center of the visible area of the image receptor.(e) For fluoroscopic equipment manufactured on or after June 10, 2006, other than radiation therapy simulation systems, the maximum area of the x-ray field in the plane of the image receptor shall conform to one of the following requirements:1. When any linear dimension of the visible area of the image receptor measured through the center of the visible area is less than or equal to 34 cm in any direction, at least 80% of the area of the x-ray field overlaps the visible area of the image receptor.2. When any linear dimension of the visible area of the image receptor measured through the center of the visible area is greater than 34 cm in any direction, the x-ray field measured along the direction of greatest misalignment with the visible area of the image receptor does not extend beyond the edge of the visible area of the image receptor by more than 2 cm.(f) For x-ray systems with inherently rectangular image receptors manufactured on or after June 10, 2006, all the following applies: 1. Neither the length nor the width of the x-ray field in the plane of the image receptor shall exceed that of the visible area of the image receptor by more than 3% of the source to image distance. The sum of the excess length and the excess width shall be no greater than 4% of the source to image distance.2. The error in alignment shall be determined along the length and width dimensions of the x-ray field which pass through the center of the visible area of the image receptor.(g) If the fluoroscopic x-ray field size is adjusted automatically as the source to image distance or image receptor size is changed, a capability may be provided for overriding the automatic adjustment in case of system failure. If it is so provided, a signal visible at the fluoroscopist's position shall indicate whenever the automatic field adjustment is overridden. Each such system failure override switch shall be clearly labeled as follows: For X-ray Field Limitation System Failure
(3) ACTIVATION OF TUBE. X-ray production in the fluoroscopic mode shall be controlled by a device which requires continuous pressure by the operator for the entire time of any exposure. When recording serial radiographic images from the fluoroscopic image receptor, the operator shall be able to terminate the x-ray exposure at any time, but means may be provided to permit completion of any single exposure of the series in process.(4) AIR KERMA RATES. (a) Fluoroscopic equipment manufactured before May 19, 1995 shall meet all the following requirements: 1. Equipment provided with automatic exposure rate control shall not be operable at any combination of tube potential and current that will result in an air kerma rate in excess of 88 mGy per minute (10 R/min) at the measurement point specified in par. (e), except as specified in par. (e) 6.2. Equipment provided without automatic exposure rate control shall not be operable at any combination of tube potential and current that will result in an air kerma rate in excess of 44 mGy per minute (5 R/min) at the measurement point specified in par. (e), except as specified in par. (e) 6.3. Equipment provided with both an automatic exposure rate control mode and a manual mode shall not be operable at any combination of tube potential and current that will result in an air kerma rate in excess of 88 mGy per minute (10 R/min) in either mode at the measurement point specified in par. (e), except as specified in par. (e) 6.4. Equipment may be modified in accordance with 21 CFR 1020.30(q) to comply with par. (a). When the equipment is modified, it shall bear a label indicating the date of the modification and the statement: Modified to comply with 21 CFR 1020.32(h) (2).
(b) The requirements of par. (a) do not apply to all the following: 1. During recording of fluoroscopic images.2. When a mode of operation has an optional high-level control, in which case that mode shall not be operable at any combination of tube potential and current that will result in an air kerma rate in excess of the rates specified in this subsection at the measurement point specified in par. (e), unless the high-level control is activated. Special means of activation of high-level controls shall be required. The high-level control shall be operable only when continuous manual activation is provided by the operator. A continuous signal audible to the fluoroscopist shall indicate that the high-level control is being employed.(c) Fluoroscopic equipment manufactured on or after May 19, 1995 shall meet all the following requirements:1. Equipped with automatic exposure rate control if operable at any combination of tube potential and current that results in an air kerma rate greater than 44 mGy per minute (5 R/min) at the measurement point specified in this subsection. Provision for manual selection of technique factors may be provided.2. Not be operable at any combination of tube potential and current that will result in an air kerma rate in excess of 88 mGy per minute (10 R/min) at the measurement point specified in par. (e)(d) The requirements of par. (c) do not apply to all the following: 1. For equipment manufactured prior to June 10, 2006, during the recording of images from a fluoroscopic image receptor using photographic film or a video camera when the x-ray source is operated in a pulsed mode.2. For equipment manufactured on or after June 10, 2006, during the recording of images from the fluoroscopic image receptor for the purpose of providing the user with a recorded image after termination of exposure. Such recording does not include images resulting from a last image-hold feature that are not recorded.3. When a mode of operation has an optional high-level control and the control is activated, in which case the equipment shall not be operable at any combination of tube potential and current that will result in an air kerma rate in excess of 176 mGy per minute (20 R/min) at the measurement point specified par. (e). Special means of activation of high-level controls shall be required. The high-level control shall be operable only when continuous manual activation is provided by the operator. A continuous signal audible to the fluoroscopist shall indicate that the high-level control is being employed.(e) Compliance with par. (c) shall be determined as follows:1. If the source is below the x-ray table, the air kerma rate shall be measured at 1 cm above the tabletop or cradle.2. If the source is above the x-ray table, the air kerma rate shall be measured at 30 cm above the tabletop with the end of the beam-limiting device or spacer positioned as closely as possible to the point of measurement.3. In a C-arm type of fluoroscope, the air kerma rate shall be measured at 30 cm from the input surface of the fluoroscopic imaging assembly, with the source positioned at any available source to image distance, provided that the end of the beam limiting device or spacer is no closer than 30 cm from the input surface of the fluoroscopic imaging assembly.4. In a C-arm type of fluoroscope having an source to image distance less than 45 cm, the air kerma rate shall be measured at the minimum source to skin distance.5. In a lateral type of fluoroscope, the air kerma rate shall be measured at a point 15 cm from the centerline of the x-ray table and in the direction of the x-ray source with the end of the beam limiting device or spacer positioned as closely as possible to the point of measurement. If the tabletop is movable, it shall be positioned as closely as possible to the lateral x-ray source, with the end of the beam-limiting device or spacer no closer than 15 cm to the centerline of the x-ray table.6. Fluoroscopic radiation therapy simulation systems are exempt from this paragraph.(5) INDICATION OF POTENTIAL AND CURRENT. During fluoroscopy and cinefluorography, x-ray tube potential and current shall be continuously indicated. Deviation of x-ray tube potential and current from the indicated values shall not exceed the maximum deviation as stated by the manufacturer in accordance with 21 CFR 1020.30(h) (3).(6) SOURCE TO SKIN DISTANCE. (a) Means shall be provided to limit the source to skin distance to not less than 38 cm on stationary fluoroscopes and to not less than 30 cm on mobile and portable fluoroscopes. In addition, for fluoroscopes intended for specific surgical application that would be prohibited at the source-skin distances specified in this paragraph, provisions may be made for operation at shorter source-skin distances but in no case less than 20 cm.(b) For stationary, mobile, or portable C-arm fluoroscopic systems manufactured on or after June 10, 2006, having a maximum source-image receptor distance of less than 45 cm, means shall be provided to limit the source-skin distance to not less than 19 cm. Such systems shall be labeled for extremity use only. In addition, for those systems intended for specific surgical application that would be prohibited at the source-skin distances specified in this paragraph, provisions may be made for operation at shorter source-skin distances but in no case less than 10 cm.(7) FLUOROSCOPIC IRRADIATION TIME, DISPLAY, AND SIGNAL. (a) Fluoroscopic equipment manufactured before June 10, 2006, shall be provided with means to preset the cumulative irradiation time of the fluoroscopic tube. The maximum cumulative time of the timing device shall not exceed 5 minutes without resetting. A signal audible to the fluoroscopist shall indicate the completion of any preset cumulative Irradiation time. Such signal shall continue to sound while x-rays are produced until the timing device is reset.(b) As an alternative to the requirements of par. (a), radiation therapy simulation systems may be provided with a means to indicate the total cumulative exposure time during which x-rays were produced, and which is capable of being reset between x-ray examinations.(c) For x-ray controls manufactured on or after June 10, 2006, all of the following shall be provided for each fluoroscopic tube: 1. A display of the fluoroscopic irradiation time at the fluoroscopist's working position.2. The display required in subd. 1. shall function independently of the audible signal described in par. (a) and meet all the following requirements: a. When the x-ray tube is activated, the fluoroscopic irradiation time in minutes and tenths of minutes shall be continuously displayed and updated at least once every 6 seconds.b. The fluoroscopic irradiation time shall also be displayed within 6 seconds of termination of an exposure and remain displayed until reset.c. Means shall be provided to reset the display to zero prior to the beginning of a new examination or procedure.3. A signal audible to the fluoroscopist shall sound for each passage of 5 minutes of fluoroscopic irradiation time during an examination or procedure. The signal shall sound until manually reset or, if automatically reset, for at least 2 seconds.(d) If fluoroscopic equipment is modified in accordance with 21 CFR 1020.30(q) to comply with the requirements in par. (a), it shall bear a label that states: Modified to comply with 21 CFR 1020.32(h)(2)
(8) MOBILE AND PORTABLE FLUOROSCOPES. Mobile and portable fluoroscopes shall use image-intensification or a direct-digital receptor.(9) DISPLAY OF LAST-IMAGE-HOLD. (a) Fluoroscopic equipment manufactured on or after June 10, 2006, shall be equipped with means to display the last image following termination of the fluoroscopic exposure.(b) For an LIH obtained by retaining pre-termination fluoroscopic images, if the number of images and method of combining images are selectable by the user, the selection shall be indicated prior to initiation of the fluoroscopic exposure.(c) For an LIH image obtained by initiating a separate radiographic-like exposure at the termination of fluoroscopic imaging, the technique factors for the LIH image shall be selectable prior to the fluoroscopic exposure, and the combination selected shall be indicated prior to initiation of the fluoroscopic exposure.(d) Means shall be provided to clearly indicate to the user whether a displayed image is the LIH radiograph or fluoroscopy. Display of the LIH radiograph shall be replaced by the fluoroscopic image concurrently with re-initiation of fluoroscopic exposure, unless separate displays are provided for the LIH radiograph and fluoroscopic images.(e) The predetermined or selectable options for producing the LIH radiograph shall be described in the information required by 21 CFR 1020.30(h). The information shall include a description of any technique factors applicable for the selected option and the impact of the selectable options on image characteristics and the magnitude of radiation emissions.(10) DISPLAYS OF VALUES OF AIR KERMA RATE AND CUMULATIVE AIR KERMA. Fluoroscopic equipment manufactured on or after June 10, 2006, shall display at the fluoroscopist's working position the air kerma rate and cumulative air kerma. Each x-ray tube used during an examination or procedure shall meet all the following requirements: (a) When the x-ray tube is activated and the number of images produced per unit time is greater than 6 images per second, the air kerma rate in mGy/min shall be continuously displayed and updated at least once every second.(b) The cumulative air kerma in units of mGy shall be displayed either within 5 seconds of termination of an exposure or displayed continuously and updated at least once every 5 seconds.(c) The display of the air kerma rate shall be clearly distinguishable from the display of the cumulative air kerma.(d)1. The air kerma rate and cumulative air kerma shall represent the value for conditions of free-in-air irradiation at one of the referenced locations.2. For fluoroscopes with x-ray source below the x-ray table, x-ray source above the table, or of lateral type, the reference locations shall be the respective locations specified in sub. (4) for measuring compliance with air kerma rate limits.3. For C-arm fluoroscopes, the reference location shall be 15 cm from the isocenter toward the x-ray source along the beam axis. Alternatively, the reference location shall be at a point specified by the manufacturer to represent the location of the intersection of the x-ray beam with the patient's skin. Note: The reference location is identified and described specifically in the information provided to users according to 21 CFR 1020.30(h) (6) (iii).
(e) Means shall be provided to reset to zero the display of cumulative air kerma prior to the commencement of a new examination or procedure.(f) The displayed air kerma rate and cumulative air kerma shall not deviate from the actual values by more than ±35 percent over the range of 6 mGy/min and 100 mGy to the maximum indication of air kerma rate and cumulative air kerma, respectively. Compliance shall be determined with an irradiation time greater than 3 seconds.(11) EQUIPMENT OPERATIONS.(a) The registrant shall ensure that only a licensed practitioner or a radiologic technologist who is trained in the safe use of fluoroscopic x-ray systems is allowed to operate these systems. All fluoroscopic x-ray images shall be viewed, directly or indirectly, and interpreted by a licensed practitioner.(b) The use of fluoroscopic x-ray systems by radiologic technologists shall be performed under the supervision of a licensed practitioner for the purpose of localization to obtain images for diagnostic purposes.(c) Radiologic technology students may not operate fluoroscopic x-ray systems except under the direct supervision of a licensed practitioner or radiologic technologist.(d) Fluoroscopic x-ray systems may not be used as a positioning tool for general purpose radiographic examinations.(e) The registrant shall require the operator of a fluoroscopic x-ray system to meet either of the following requirements:1. Is certified by the American Board of Radiology or board eligible.2. Has completed training to include the following:a. Principles and operation of the fluoroscopic x-ray system.b. Biological effects of x-ray.c. Principles of radiation protection.e. High level control options.f. Dose reduction techniques for fluoroscopic x-ray systems.g. Applicable state and federal regulations.(12) AIR KERMA MEASUREMENTS. Annual measurements of both typical and maximum air kerma shall be made by a medical physicist or a person approved by a medical physicist.Wis. Admin. Code Department of Health Services DHS 157.76
CR 01-108: cr. Register July 2002 No. 559, eff. 8-1-02; CR 06-021: r. and recr. Register October 2006 No. 610, eff. 11-1-06; CR 09-062: cr. (11) and (12) Register April 2010 No. 652, eff. 5-1-10.Amended by, CR 16-078: r. and recr. (7) (c), cr. (7) (d), am. (11) (a) Register January 2018 No. 745, eff. 2-1-18; correction in (7) (c) 2. made under s. 35.17, Stats., Register January 2018 No. 745, eff. 2/1/2018Amended by, CR 22-015: am. (intro.), (2) (b), (8) Register June 2023 No. 810, eff. 7/1/2023Materials should be placed in the useful beam to protect the imaging system when conducting these periodic measurements. Air kerma measurements do not include backscatter.