ClearanceBrief
510(k) K830410 ยท DSP System, Balloon, Intra-Aortic And Control

EK COMBI MSG-1

ApplicantJedmed Instrument Co., Walker MI, US
DecisionSubstantially Equivalent, Apr 27, 1983
ReceivedFeb 8, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830410

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.