FDA 510(k) Application Details - K961579

Device Classification Name	Instrument, Coagulation, Automated   More FDA Info for this Device
510(K) Number	K961579
Device Name	Instrument, Coagulation, Automated
Applicant	AMERICAN BIOPRODUCTS CO. 5 CENTURY DR. PARSIPPANY, NJ 07054 US Other 510(k) Applications for this Company
Contact	ANDREW LOC B LE, PH.D. Other 510(k) Applications for this Contact
Regulation Number	864.5400   More FDA Info for this Regulation Number
Classification Product Code	GKP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/24/1996
Decision Date	07/10/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	HE - Hematology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review