ClearanceBrief
510(k) K100921 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

ADMIRAL XTREME PTA BALLOON DILATATION CATHETER

ApplicantInvatec S.P.A., Bethlehem PA, US
DecisionSubstantially Equivalent, Apr 30, 2010
ReceivedApr 2, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K100921

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.