ClearanceBrief
510(k) K912317 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO PTA CATH

ApplicantSchneider Intl., Ltd., Plymouth MN, US
DecisionSubstantially Equivalent, Aug 22, 1991
ReceivedMay 24, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912317

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.