ClearanceBrief
510(k) K945693 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

CVD PERIFLOW(TM) (SMALL VESSEL) BALLOON DILATATION CATHETER

ApplicantCardiovascular Dynamics, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Aug 17, 1995
ReceivedNov 21, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945693

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.