ClearanceBrief
510(k) K903736 ยท DSP System, Balloon, Intra-Aortic And Control

DATASCOPE PERCOR STAT DL10.5 FR40CC IN AORTIC BAL

ApplicantDatascope Corp., Oakland NJ, US
DecisionSubstantially Equivalent, Oct 9, 1990
ReceivedAug 16, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903736

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.