ClearanceBrief
510(k) K131553 ยท CAC Apparatus, Autotransfusion

XTRA

ApplicantSorin Group Deutschland GmbH, Waltham MA, US
DecisionSubstantially Equivalent, Mar 21, 2014
ReceivedMay 30, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K131553

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.