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REAGENT GPT, ENZYME

K770314 Class I Traditional
Decision Date
1977-03-30
Sponsor / Applicant
Icn Pharmaceuticals, Inc.

Technical Specification

510(k) Submission ID K770314
Product Code CKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1030
Decision Date 1977-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REAGENT GPT, ENZYME received FDA 510(k) clearance under submission number K770314, sponsored by Icn Pharmaceuticals, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1977-03-30.

Classification & Regulation

This clearance is catalogued under FDA product code CKA and 21 CFR 862.1030, within the Clinical Chemistry review panel as a Class I device.