ClearanceBrief
510(k) K925661 ยท KRL Detector, Bubble, Cardiopulmonary Bypass

STOCKERT CAPS1 CARDIOPLEGIC CONTROL MODULE

ApplicantSorin Biomedica, Fiat, USA, Inc., Irvine CA, US
DecisionSubstantially Equivalent, May 18, 1993
ReceivedNov 10, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925661

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.