ClearanceBrief
510(k) K851987 ยท DRS Transducer, Blood-Pressure, Extravascular

FLUSH DEVICE, AUTOMATIC

ApplicantTransamerica Delaval, Inc., Pasadena CA, US
DecisionSubstantially Equivalent, Aug 16, 1985
ReceivedMay 7, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851987

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.