ClearanceBrief
510(k) K915349 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

PTA BALLOON CATHETER

ApplicantSchneider Intl., Ltd., Plymouth MN, US
DecisionSubstantially Equivalent, Feb 11, 1992
ReceivedNov 26, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915349

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.