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CLEARBLUE EASY EASY READ PREGNANCY TEST

K041404 Class II Special
Decision Date
2004-06-08
Sponsor / Applicant
Unipath , Ltd.

Technical Specification

510(k) Submission ID K041404
Product Code LCX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 2004-06-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEARBLUE EASY EASY READ PREGNANCY TEST received FDA 510(k) clearance under submission number K041404, sponsored by Unipath , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2004-06-08.

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.