Reagent Set, U.V. Enzmatic Kinetic, Sgot

FDA 510(k) K781725 · Medical Analysis Systems, Inc.

Substantially Equivalent

510(k) numberK781725

Submission

Device name
Reagent Set, U.V. Enzmatic Kinetic, Sgot
Applicant
Medical Analysis Systems, Inc.
Mchenry, IL, US
Received
October 11, 1978
Decision date
November 3, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Reagent Set, U.V. Enzmatic Kinetic, Sgot cleared by the FDA?

Reagent Set, U.V. Enzmatic Kinetic, Sgot (K781725) received a 510(k) decision of Substantially Equivalent on November 3, 1978, 23 days after the submission was received.

What is the product code of K781725?

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