ClearanceBrief
510(k) K882925 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

ACS SCHWARTEN XT BALLOON DILATATION CATHETER

ApplicantAdvanced Cardiovascular Systems, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, Sep 28, 1988
ReceivedJul 13, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882925

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.