ClearanceBrief
510(k) K955742 ยท DXC Clamp, Vascular

D. DEVICE II

ApplicantYousef Daneshvar, Livonia MI, US
DecisionSubstantially Equivalent, Aug 12, 1996
ReceivedDec 19, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955742

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.