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SERUM GLUTAMIC-PYRUVIC TRANSAMINASE

K780507 Class I Traditional
Decision Date
1978-05-03
Sponsor / Applicant
Gamma Enterprises, Inc.

Technical Specification

510(k) Submission ID K780507
Product Code CKC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1030
Decision Date 1978-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SERUM GLUTAMIC-PYRUVIC TRANSAMINASE received FDA 510(k) clearance under submission number K780507, sponsored by Gamma Enterprises, 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 1978-05-03.

Classification & Regulation

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