ClearanceBrief
510(k) K850394 ยท DWS Instruments, Surgical, Cardiovascular

LEMAITRE RETROGRADE VALVULOTOME-MANU-SURGICA INSTR

ApplicantVascutech, Inc., Washington DC, US
DecisionSubstantially Equivalent, Apr 24, 1985
ReceivedFeb 1, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850394

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.