ClearanceBrief
510(k) K053398 ยท DXC Clamp, Vascular

COMPASS COMPRESSION ASSIST HANDLE

ApplicantSemler Technologies, Inc. Dba, Portland OR, US
DecisionSubstantially Equivalent, Mar 10, 2006
ReceivedDec 6, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K053398

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.