ClearanceBrief
510(k) K903930 ยท DSP System, Balloon, Intra-Aortic And Control

DATASCOPE PERCOR STAT DL 10.5 FR 50CC

ApplicantDatascope Corp., Oakland NJ, US
DecisionSubstantially Equivalent, Nov 16, 1990
ReceivedAug 24, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903930

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.