ClearanceBrief
510(k) K913773 ยท CAC Apparatus, Autotransfusion

COBE BRAT SYSTEMS WITHOUT REINFUSION PROTECTION

ApplicantCobe Cardiovascular, Inc., Arvada CO, US
DecisionSubstantially Equivalent, Jan 27, 1992
ReceivedAug 23, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913773

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.