ClearanceBrief
510(k) K123358 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

PACIFIC PLUS

ApplicantMedtronic Vascular, Santa Rosa CA, US
DecisionSubstantially Equivalent, Jan 29, 2013
ReceivedOct 31, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123358

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.