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CREATININE REAGENT(CREAT), CAT.# RE0015/MODIFIED

K910147 Class II Traditional
Decision Date
1991-03-11
Sponsor / Applicant
Olympus Corp.

Technical Specification

510(k) Submission ID K910147
Product Code CGX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1225
Decision Date 1991-03-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CREATININE REAGENT(CREAT), CAT.# RE0015/MODIFIED received FDA 510(k) clearance under submission number K910147, sponsored by Olympus Corp.. 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 1991-03-11.

Classification & Regulation

This clearance is catalogued under FDA product code CGX and 21 CFR 862.1225, within the Clinical Chemistry review panel as a Class II device.