ClearanceBrief
510(k) K952064 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

FOCUS BALLOON DILATATION CATHETER

ApplicantCardiovascular Dynamics, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Jun 21, 1995
ReceivedMay 2, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952064

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.