ClearanceBrief
510(k) K173894 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

Jade PTA Balloon Dilatation Catheter

ApplicantOrbusneich Medical Trading, Inc., Fort Lauderdale FL, US
DecisionSubstantially Equivalent, Feb 9, 2018
ReceivedDec 21, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173894

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.