21 CFR Part 862 · Clinical Chemistry and Clinical Toxicology Devices

§ 862.3280 Clinical toxicology control material

Subpart D - Clinical Toxicology Test Systems Official text on eCFR Amendment history

(a) Identification. A clinical toxicology control material is a device intended to provide an estimation of the precision of a device test system and to detect and monitor systematic deviations from accuracy resulting from reagent or instrument defects. This generic type of device includes various single, and multi-analyte control materials.

(b) Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 862.9 .

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FDA guidance that cites § 862.3280

Amendment history

Federal Register documents that created or amended this section.