ClearanceBrief
510(k) K833594 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

FUKUDA DENSHI FX-302 AUTO/THREE CHAN

ApplicantBrentwood Instruments, Inc., Walker MI, US
DecisionSubstantially Equivalent, Sep 11, 1984
ReceivedOct 12, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833594

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.