ClearanceBrief
510(k) K772332 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

MONITOR, CARDIAC, BEDSIDE

ApplicantTelectronics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 13, 1978
ReceivedDec 22, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772332

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.