ClearanceBrief
510(k) K924894 ยท CAC Apparatus, Autotransfusion

AUTOVAC 7900 SERIES

ApplicantBoehringer Laboratories, Norristown PA, US
DecisionSubstantially Equivalent, Feb 5, 1993
ReceivedSep 28, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924894

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.