ClearanceBrief
510(k) K983830 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

COPPERHEAD 5 FR. PTA CATHETER, FINCH 4 FR. PTA CATHETER

ApplicantMallinckroot, Inc., St Louis MO, US
DecisionSubstantially Equivalent, Apr 16, 1999
ReceivedOct 30, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983830

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.