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REAGENT, TRIGLY. C-ZYME NDC#12739-0017-1

K760195 Class I Traditional
Decision Date
1976-08-03
Sponsor / Applicant
Coulter Electronics, Inc.

Technical Specification

510(k) Submission ID K760195
Product Code CDT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1705
Decision Date 1976-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REAGENT, TRIGLY. C-ZYME NDC#12739-0017-1 received FDA 510(k) clearance under submission number K760195, sponsored by Coulter Electronics, 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 1976-08-03.

Classification & Regulation

This clearance is catalogued under FDA product code CDT and 21 CFR 862.1705, within the Clinical Chemistry review panel as a Class I device.