ClearanceBrief
510(k) K926271 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIO

ApplicantSchneider Intl., Ltd., Plymouth MN, US
DecisionSubstantially Equivalent, Jun 7, 1993
ReceivedDec 18, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926271

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.