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TOTAL T3 ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1005

K991311 Class II Traditional
Decision Date
1999-06-02
Sponsor / Applicant
Biocheck, Inc.

Technical Specification

510(k) Submission ID K991311
Product Code CDP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1710
Decision Date 1999-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL T3 ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1005 received FDA 510(k) clearance under submission number K991311, sponsored by Biocheck, 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 1999-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code CDP and 21 CFR 862.1710, within the Clinical Chemistry review panel as a Class II device.