ClearanceBrief
510(k) K854505 ยท DRS Transducer, Blood-Pressure, Extravascular

CARDIMAX FX-406U

ApplicantBrentwood Instruments, Inc., Torrance CA, US
DecisionSubstantially Equivalent, Feb 4, 1986
ReceivedNov 12, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854505

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.