ClearanceBrief
510(k) K945943 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

CVD PERIFLOW(TM) BALLOON DILATATION CATHETER

ApplicantCardio-Dynamics, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Feb 24, 1995
ReceivedDec 5, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945943

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.