FDA 510(k) Application Details - K960517

Device Classification Name Catheter, Angioplasty, Peripheral, Transluminal

  More FDA Info for this Device
510(K) Number K960517
Device Name Catheter, Angioplasty, Peripheral, Transluminal
Applicant C.R. BARD, INC.
13183 HARLAND DRIVE
COVINGTON, GA 30014-6421 US
Other 510(k) Applications for this Company
Contact DONNA J WILSON
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 02/05/1996
Decision Date 04/09/1996
Decision SESE - SUBST EQUIV
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact