Cleared Traditional

K904004 - AMRESCOCREAT KINASE REAGENT 7716/17,7516,7416,7116
(FDA 510(k) Clearance)

Dec 1990
Decision
104d
Days
Class 2
Risk

K904004 is an FDA 510(k) clearance for the AMRESCOCREAT KINASE REAGENT 7716/17,7516,7416,7116. This device is classified as a Nad Reduction/nadh Oxidation, Cpk Or Isoenzymes (Class II - Special Controls, product code CGS).

Submitted by Amresco, Inc. (Solon, US). The FDA issued a Cleared decision on December 11, 1990, 104 days after receiving the submission on August 29, 1990.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1215.

Submission Details

510(k) Number K904004 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 29, 1990
Decision Date December 11, 1990
Days to Decision 104 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code CGS — Nad Reduction/nadh Oxidation, Cpk Or Isoenzymes
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1215

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