ClearanceBrief
510(k) K924171 ยท MGZ Valvulotome

LEMAITRE RETROGRADE VALVULOTOME

ApplicantVascutech, Inc., Andover MA, US
DecisionSubstantially Equivalent, Feb 16, 1993
ReceivedAug 18, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924171

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.