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AUTOBEAD TSH ENZYME IMMUNOASSAY REAGENT KIT

K930006 Class II Traditional
Decision Date
1993-09-09
Sponsor / Applicant
Bio-Chem Laboratory Systems, Inc.

Technical Specification

510(k) Submission ID K930006
Product Code JLW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1690
Decision Date 1993-09-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTOBEAD TSH ENZYME IMMUNOASSAY REAGENT KIT received FDA 510(k) clearance under submission number K930006, sponsored by Bio-Chem Laboratory Systems, 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 1993-09-09.

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.