ClearanceBrief
510(k) K921943 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO (PTA) BAL

ApplicantSchneider Intl., Ltd., Plymouth MN, US
DecisionSubstantially Equivalent, Jun 17, 1992
ReceivedApr 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921943

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.