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ACCUWELL TSH, MODEL KAW-TSH-960

K001455 Class II Traditional
Decision Date
2000-11-02
Sponsor / Applicant
Neometrics, Inc.

Technical Specification

510(k) Submission ID K001455
Product Code JLW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1690
Decision Date 2000-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCUWELL TSH, MODEL KAW-TSH-960 received FDA 510(k) clearance under submission number K001455, sponsored by Neometrics, 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 2000-11-02.

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.