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ASTRA TOTAL PROTEIN REAGENT

K813536 Class II Traditional
Decision Date
1981-12-31
Sponsor / Applicant
Hi Chem, Inc.

Technical Specification

510(k) Submission ID K813536
Product Code CEK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1635
Decision Date 1981-12-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASTRA TOTAL PROTEIN REAGENT received FDA 510(k) clearance under submission number K813536, sponsored by Hi Chem, 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 1981-12-31.

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.