FDA 510(k) Application Details - K960316

Device Classification Name	Kit, Test, Pregnancy, Hcg, Over The Counter   More FDA Info for this Device
510(K) Number	K960316
Device Name	Kit, Test, Pregnancy, Hcg, Over The Counter
Applicant	UNIPATH LTD. NORSE ROAD BEDFORD MK41 OQG GB Other 510(k) Applications for this Company
Contact	Louise Roberts Other 510(k) Applications for this Contact
Regulation Number	862.1155   More FDA Info for this Regulation Number
Classification Product Code	LCX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/23/1996
Decision Date	04/29/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review