ClearanceBrief
510(k) K834530 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

EXTENSION BOX EB200

ApplicantHoneywell, Inc., Walker MI, US
DecisionSubstantially Equivalent, Jun 1, 1984
ReceivedDec 21, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834530

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.