ClearanceBrief
510(k) K903392 ยท CAC Apparatus, Autotransfusion

ELECTROMEDICS BT422-120 AND BT422-40

ApplicantElectromedics, Inc., Englewood CO, US
DecisionSubstantially Equivalent, Sep 6, 1990
ReceivedJul 27, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903392

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.