FDA 510(k) Application Details - K073434

Device Classification Name	Introducer, Catheter   More FDA Info for this Device
510(K) Number	K073434
Device Name	Introducer, Catheter
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	870.1340   More FDA Info for this Regulation Number
Classification Product Code	DYB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/06/2007
Decision Date	04/01/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review