ClearanceBrief
510(k) K960445 ยท DYB Introducer, Catheter

INPUT TUOHY-BORST LOCKING DEVICE

ApplicantC.R. Bard, Inc., Billerica MA, US
DecisionSubstantially Equivalent, Aug 12, 1996
ReceivedFeb 1, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960445

No recall in the FDA data names this 510(k).

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