ClearanceBrief
510(k) K221491 ยท DWA Control, Pump Speed, Cardiopulmonary Bypass

Anivia SG1000 Pump Console

ApplicantApmtd, Inc., Wilmington MA, US
DecisionSubstantially Equivalent, Feb 3, 2023
ReceivedMay 23, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221491

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.