510(k) K993333

CLEARPLAN EASY II HOME PREGNANCY TEST by Unipath , Ltd. — Product Code LCX

K993333 is an FDA 510(k) premarket notification submitted by Unipath , Ltd. for the device "CLEARPLAN EASY II HOME PREGNANCY TEST". The FDA issued a decision of Substantially Equivalent on December 16, 1999. 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
December 16, 1999
Date Received
October 4, 1999
Clearance Type
Traditional
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