meddevicedb.com FDA Device Reference

SYSTEM 5 - SEMI-AUTOMATED CLIN. ANALY

K760749 Class I Traditional
Decision Date
1976-12-29
Sponsor / Applicant
Gilford Instrument Laboratories, Inc.

Technical Specification

510(k) Submission ID K760749
Product Code JJC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2150
Decision Date 1976-12-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYSTEM 5 - SEMI-AUTOMATED CLIN. ANALY received FDA 510(k) clearance under submission number K760749, sponsored by Gilford Instrument Laboratories, 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 1976-12-29.

Classification & Regulation

This clearance is catalogued under FDA product code JJC and 21 CFR 862.2150, within the Clinical Chemistry review panel as a Class I device.