ClearanceBrief
510(k) K053021 ยท DTS Sucker, Cardiotomy Return, Cardiopulmonary Bypass

ESTECH CLEARVIEW MV ATRIAL DEPRESSOR

ApplicantEstech, Inc., Alameda CA, US
DecisionSubstantially Equivalent, Jan 26, 2006
ReceivedOct 26, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K053021

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.