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REAGENT FOR DETERM. GLUTAMIC-PYRUVIC-

K800689 Class I Traditional
Decision Date
1980-05-30
Sponsor / Applicant
Diagnostic Solutions, Inc.

Technical Specification

510(k) Submission ID K800689
Product Code CKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1030
Decision Date 1980-05-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REAGENT FOR DETERM. GLUTAMIC-PYRUVIC- received FDA 510(k) clearance under submission number K800689, sponsored by Diagnostic Solutions, 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 1980-05-30.

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.