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BIO-RAD TOTAL PROTEIN TEST KIT

K913315 Class I Traditional
Decision Date
1992-01-02
Sponsor / Applicant
Bio-Rad

Technical Specification

510(k) Submission ID K913315
Product Code CEF
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1630
Decision Date 1992-01-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIO-RAD TOTAL PROTEIN TEST KIT received FDA 510(k) clearance under submission number K913315, sponsored by Bio-Rad. 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 1992-01-02.

Classification & Regulation

This clearance is catalogued under FDA product code CEF and 21 CFR 862.1630, within the Clinical Chemistry review panel as a Class I device.