FDA 510(k) Application Details - K014028

Device Classification Name	Activated Partial Thromboplastin   More FDA Info for this Device
510(K) Number	K014028
Device Name	Activated Partial Thromboplastin
Applicant	CARESIDE HEMOTOLOGY, INC. 6100 BRISTOL PKWY. CULVER CITY, CA 90230 US Other 510(k) Applications for this Company
Contact	KENNETH B ASARCH Other 510(k) Applications for this Contact
Regulation Number	864.7925   More FDA Info for this Regulation Number
Classification Product Code	GFO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/06/2001
Decision Date	02/08/2002
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