ClearanceBrief
510(k) K843533 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

CARDIAC EVENT RECORDER

ApplicantCryo2 Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 28, 1985
ReceivedSep 7, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843533

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.