FDA 510(k) Application Details - K012950

Device Classification Name	Injector And Syringe, Angiographic   More FDA Info for this Device
510(K) Number	K012950
Device Name	Injector And Syringe, Angiographic
Applicant	MEDRAD, INC. ONE MEDRAD DR. INDIANOLA, PA 15051 US Other 510(k) Applications for this Company
Contact	LORRAINE R FREDES Other 510(k) Applications for this Contact
Regulation Number	870.1650   More FDA Info for this Regulation Number
Classification Product Code	DXT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/04/2001
Decision Date	10/04/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review	Y