FDA 510(k) Application Details - K030533

Device Classification Name	Kit, Test, Pregnancy, Hcg, Over The Counter   More FDA Info for this Device
510(K) Number	K030533
Device Name	Kit, Test, Pregnancy, Hcg, Over The Counter
Applicant	CENOGENICS CORP. 100 RT. 520 MORGANVILLE, NJ 07751 US Other 510(k) Applications for this Company
Contact	NITZ KATZ 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	02/14/2003
Decision Date	04/17/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review