21 CFR Part 862 · Clinical Chemistry and Clinical Toxicology Devices

§ 862.1660 Quality control material (assayed and unassayed)

Subpart B - Clinical Chemistry Test Systems Official text on eCFR Amendment history

(a) Identification. A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls.

(b) Classification. Class I (general controls). Except when intended for use in donor screening tests, quality control materials (assayed and unassayed) are 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 § 862.1660

Amendment history

Federal Register documents that created or amended this section.