ClearanceBrief
510(k) K922610 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

BALLOON DILATATION CATHETER

ApplicantBoston Scientific Corp, San Jose CA, US
DecisionSubstantially Equivalent, Nov 18, 1992
ReceivedJun 2, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922610

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.