ClearanceBrief
510(k) K902453 ยท DRS Transducer, Blood-Pressure, Extravascular

OSCILLOMETRIC PULSE DETECTION DEVICE

ApplicantThomas J. Fogarty, M.D., Portola Valley CA, US
DecisionSubstantially Equivalent, Aug 23, 1990
ReceivedJun 1, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902453

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.