FDA 510(k) Application Details - K980087

Device Classification Name	Clamp, Vascular   More FDA Info for this Device
510(K) Number	K980087
Device Name	Clamp, Vascular
Applicant	PRESSURE PRODUCTS, INC. 30423 MIRALESTE DR. RANCHO PALOS VERDES, CA 90275 US Other 510(k) Applications for this Company
Contact	JAMES BARLEY Other 510(k) Applications for this Contact
Regulation Number	870.4450   More FDA Info for this Regulation Number
Classification Product Code	DXC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/09/1998
Decision Date	07/01/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review