meddevicedb.com FDA Device Reference

SERUM, GLUTAMIC-PYRUVIC

K790016 Class I Traditional
Decision Date
1979-02-15
Sponsor / Applicant
Fisher Scientific Co., LLC

Technical Specification

510(k) Submission ID K790016
Product Code CKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1030
Decision Date 1979-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SERUM, GLUTAMIC-PYRUVIC received FDA 510(k) clearance under submission number K790016, sponsored by Fisher Scientific Co., LLC. 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 1979-02-15.

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.