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TOTAL PROTEIN REAGENT FOR ASTRA 8 STAT/ROU ANALYZE

K853244 Class II Traditional
Decision Date
1985-08-12
Sponsor / Applicant
Simmler, Inc.

Technical Specification

510(k) Submission ID K853244
Product Code CEK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1635
Decision Date 1985-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL PROTEIN REAGENT FOR ASTRA 8 STAT/ROU ANALYZE received FDA 510(k) clearance under submission number K853244, sponsored by Simmler, 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 1985-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code CEK and 21 CFR 862.1635, within the Clinical Chemistry review panel as a Class II device.