FDA 510(k) Application Details - K780438

Device Classification Name Wire, Guide, Catheter

  More FDA Info for this Device
510(K) Number K780438
Device Name Wire, Guide, Catheter
Applicant C.R. BARD, INC.

, US
Other 510(k) Applications for this Company
Regulation Number 870.1330

  More FDA Info for this Regulation Number
Classification Product Code DQX
Other 510(k) Applications for this Device

  More FDA Info for this Product Code
Date Received 03/20/1978
Decision Date 06/28/1978
Decision SE - Substantially Equivalent
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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