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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name kit, test, pregnancy, hcg, over the counter
510(k) Number K060128
Device Name CLEARBLUE EASY DIGITAL PREGNANCY TEST
Applicant
UNIPATH LTD.
PRIORY BUSINESS PARK
bedford,  GB mk44 3up
Applicant Contact louise roberts
Correspondent
UNIPATH LTD.
PRIORY BUSINESS PARK
bedford,  GB mk44 3up
Correspondent Contact louise roberts
Regulation Number862.1155
Classification Product Code
LCX  
Date Received01/18/2006
Decision Date 05/25/2006
Decision substantially equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
statement statement
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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