Olympus Aspartate Aminotransferase Reagent

FDA 510(k) K922885 · Olympus Corp.

Substantially Equivalent

510(k) numberK922885

Submission

Device name
Olympus Aspartate Aminotransferase Reagent
Applicant
Olympus Corp.
Lake Success, NY, US
Received
June 16, 1992
Decision date
July 28, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CIT – Nadh Oxidation/Nad Reduction, Ast/Sgot
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1100
Specialty
Clinical Chemistry

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Questions and answers

When was Olympus Aspartate Aminotransferase Reagent cleared by the FDA?

Olympus Aspartate Aminotransferase Reagent (K922885) received a 510(k) decision of Substantially Equivalent on July 28, 1992, 42 days after the submission was received.

What is the product code of K922885?

The FDA product code is CIT – Nadh Oxidation/Nad Reduction, Ast/Sgot, a Class II (moderate risk) device regulated under 21 CFR 862.1100.