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CREATINE KINASE UV REAGENT SET

K905588 Class II Traditional
Decision Date
1991-01-17
Sponsor / Applicant
Biochemical Trade, Inc.

Technical Specification

510(k) Submission ID K905588
Product Code JHW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 1991-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CREATINE KINASE UV REAGENT SET received FDA 510(k) clearance under submission number K905588, sponsored by Biochemical Trade, 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 1991-01-17.

Classification & Regulation

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