meddevicedb.com FDA Device Reference

SYSTEMATE GGT (EPOS APPLICATION) #65414

K905662 Class I Traditional
Decision Date
1991-01-04
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K905662
Product Code JQB
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1360
Decision Date 1991-01-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYSTEMATE GGT (EPOS APPLICATION) #65414 received FDA 510(k) clearance under submission number K905662, sponsored by Em Diagnostic Systems, 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 1991-01-04.

Classification & Regulation

This clearance is catalogued under FDA product code JQB and 21 CFR 862.1360, within the Clinical Chemistry review panel as a Class I device.