ClearanceBrief
510(k) K897126 ยท CAC Apparatus, Autotransfusion

ATRIUM 2050 CHEST DRAIN BLOOD RECOVERY SYSTEM

ApplicantAtrium Medical Corp., Hollis NH, US
DecisionSubstantially Equivalent, Mar 13, 1990
ReceivedDec 26, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K897126

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.