ClearanceBrief
510(k) K041525 ยท CAC Apparatus, Autotransfusion

HEMOVAC BLOOD REINFUSION SYSTEM

ApplicantZimmer, Inc., Dover OH, US
DecisionSubstantially Equivalent, Oct 14, 2004
ReceivedJun 8, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K041525

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.