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CLEARBLUE EASY PREGNANCY TEST

K110433 Class II Special
Decision Date
2011-05-12
Sponsor / Applicant
SPD Development Company Limited

Technical Specification

510(k) Submission ID K110433
Product Code LCX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 2011-05-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEARBLUE EASY PREGNANCY TEST received FDA 510(k) clearance under submission number K110433, sponsored by SPD Development Company Limited. 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 2011-05-12.

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.