ClearanceBrief
510(k) K875175 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

MODIFIED PERIPHERAL DILATATION CATHETERS

ApplicantSchneider-Shilley (Usa), Minneapolis MN, US
DecisionSubstantially Equivalent, Jul 28, 1988
ReceivedDec 17, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K875175

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.