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REAGENT SET, U.V. ENZMATIC KINETIC, SGOT

K781725 Class II Traditional
Decision Date
1978-11-03
Sponsor / Applicant
Medical Analysis Systems, Inc.

Technical Specification

510(k) Submission ID K781725
Product Code CIT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1100
Decision Date 1978-11-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REAGENT SET, U.V. ENZMATIC KINETIC, SGOT received FDA 510(k) clearance under submission number K781725, sponsored by Medical Analysis Systems, 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 1978-11-03.

Classification & Regulation

This clearance is catalogued under FDA product code CIT and 21 CFR 862.1100, within the Clinical Chemistry review panel as a Class II device.