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OLYMPUS CREATINE KINASE REAGENT OSR6179/6279

K994189 Class II Traditional
Decision Date
2000-01-20
Sponsor / Applicant
Olympus Diagnostica GmbH

Technical Specification

510(k) Submission ID K994189
Product Code CGS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 2000-01-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OLYMPUS CREATINE KINASE REAGENT OSR6179/6279 received FDA 510(k) clearance under submission number K994189, sponsored by Olympus Diagnostica GmbH. 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 2000-01-20.

Classification & Regulation

This clearance is catalogued under FDA product code CGS and 21 CFR 862.1215, within the Clinical Chemistry review panel as a Class II device.