ClearanceBrief
510(k) K954205 ยท MCW Catheter, Peripheral, Atherectomy

THE AMPLATZ THROMBECTOMY DEVICE

ApplicantMicrovena Corp., White Bear Lake MN, US
DecisionSubstantially Equivalent, Aug 13, 1996
ReceivedSep 7, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954205

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.