510(k) K013372

CLEARBLUE EASY EARLY RESULT PREGNANCY TEST by Unipath , Ltd. — Product Code LCX

K013372 is an FDA 510(k) premarket notification submitted by Unipath , Ltd. for the device "CLEARBLUE EASY EARLY RESULT PREGNANCY TEST". The FDA issued a decision of Substantially Equivalent on November 9, 2001. The device falls under product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter), a Class II device regulated under 21 CFR 862.1155. Unipath , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 9, 2001
Date Received
October 11, 2001
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Test, Pregnancy, Hcg, Over The Counter
Device Class
Class II
Regulation Number
862.1155
Review Panel
CH
Submission Type