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TSH ENZYME IMMUNOASSAY TEST KIT, MODEL #BC-1001

K991146 Class II Traditional
Decision Date
1999-06-22
Sponsor / Applicant
Biocheck, Inc.

Technical Specification

510(k) Submission ID K991146
Product Code JLW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1690
Decision Date 1999-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TSH ENZYME IMMUNOASSAY TEST KIT, MODEL #BC-1001 received FDA 510(k) clearance under submission number K991146, 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 1999-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code JLW and 21 CFR 862.1690, within the Clinical Chemistry review panel as a Class II device.