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BEST PREGNANCY TEST

K953606 Class II Traditional
Decision Date
1996-03-22
Sponsor / Applicant
Ameritek, Inc.

Technical Specification

510(k) Submission ID K953606
Product Code LCX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1996-03-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BEST PREGNANCY TEST received FDA 510(k) clearance under submission number K953606, sponsored by Ameritek, 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 1996-03-22.

Classification & Regulation

This clearance is catalogued under FDA product code LCX and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.