FDA 510(k) Application Details - K041293

Device Classification Name	Catheter, Angioplasty, Peripheral, Transluminal   More FDA Info for this Device
510(K) Number	K041293
Device Name	Catheter, Angioplasty, Peripheral, Transluminal
Applicant	BIPORE, INC. 31 INDUSTRIAL PKWY. NORTHVALE, NJ 07647 US Other 510(k) Applications for this Company
Contact	KEITH PALUCH Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	LIT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/14/2004
Decision Date	07/09/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review