ClearanceBrief
510(k) K932092 ยท DQO Catheter, Intravascular, Diagnostic

USCI ANGIOGRAPHIC CATHETER

ApplicantC.R. Bard, Inc., Billerica MA, US
DecisionSubstantially Equivalent, Jul 29, 1993
ReceivedApr 30, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932092

DateFirm and productCodeLinked 510(k)
Feb 10, 2004Medtronic, Inc.
Medtronic SiteSeer 5 F Tight Radius 145 Pigtail Cardiovascular Angiographic Catheter Item Number: 5A0029
Terminated
DQONone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.