ClearanceBrief
510(k) K823739 ยท DSP System, Balloon, Intra-Aortic And Control

INTRA-AORTIC BALLOON SYSTEM

ApplicantSmec, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 18, 1983
ReceivedDec 13, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823739

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.