ClearanceBrief
510(k) K002767 ยท DXC Clamp, Vascular

COMPRESSAR FEMORAL ACCESS COMPRESSION DEVICE

ApplicantSemler Technologies, Inc., Vancouver WA, US
DecisionSubstantially Equivalent, Sep 27, 2000
ReceivedSep 6, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K002767

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.