ClearanceBrief
510(k) K121385 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

VECTOR

ApplicantR4 Vascular, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Jun 14, 2012
ReceivedMay 8, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121385

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.