ClearanceBrief
510(k) K981906 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

MODIFICATION FOR PTA BALLOON CATHETER

ApplicantCook, Inc., Bloomington IN, US
DecisionSubstantially Equivalent, Jun 29, 1998
ReceivedJun 1, 1998
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K981906

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.