ClearanceBrief
510(k) K905698 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

CORDIS OPTA 5

ApplicantCordis Corp., Miami Lakes FL, US
DecisionSubstantially Equivalent, Jul 9, 1991
ReceivedDec 20, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905698

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.