ClearanceBrief
510(k) K971579 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

CORDIS OPTA 5 PTA BALLOON CATHETER

ApplicantCordis Corp., Miami Lakes FL, US
DecisionSubstantially Equivalent, Jul 18, 1997
ReceivedApr 21, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K971579

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.