ClearanceBrief
510(k) K810297 ยท DSP System, Balloon, Intra-Aortic And Control

DATASCOPE PERCOR=DL DUAL-LUMEN INTRA

ApplicantDatascope Corp., Mchenry IL, US
DecisionSubstantially Equivalent, May 6, 1981
ReceivedFeb 5, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810297

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.