meddevicedb.com FDA Device Reference

DYNAZYME II GPT 340

K771152 Class I Traditional
Decision Date
1977-11-03
Sponsor / Applicant
J.T. Baker Chemical Co.

Technical Specification

510(k) Submission ID K771152
Product Code CKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1030
Decision Date 1977-11-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DYNAZYME II GPT 340 received FDA 510(k) clearance under submission number K771152, sponsored by J.T. Baker Chemical Co.. 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 1977-11-03.

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.