21 C.F.R. § 866.5910

Current through September 30, 2024
Section 866.5910 - Quality control material for cystic fibrosis nucleic acid assays
(a)Identification. Quality control material for cystic fibrosis nucleic acid assays. A quality control material for cystic fibrosis nucleic acid assays is a device intended to help monitor reliability of a test system by detecting analytical deviations such as those that may arise from reagent or instrument variation in genetic testing. This type of device includes recombinant, synthetic, and cell line-based DNA controls.
(b)Classification. Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 866.9 . The special control is FDA's guidance document entitled "Class II Special Controls Guidance Document: Quality Control Material for Cystic Fibrosis Nucleic Acid Assays." See § 866.1(e) for the availability of this guidance document.

21 C.F.R. §866.5910

72 FR 1176, Jan. 10, 2007, as amended at 84 FR 71811, Dec. 30, 2019
As amended at 84 FR 71811, 12/30/2019