ClearanceBrief
510(k) K103751 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

MUSTANG BALLOON DILATATION CATHETERS

ApplicantBoston Scientific, Maple Grove MN, US
DecisionSubstantially Equivalent, Mar 22, 2011
ReceivedDec 23, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K103751

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.