ClearanceBrief
510(k) K780702 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

CSS-60 DIGITAL HEART RATE METER

ApplicantBurdick Corp., Mchenry IL, US
DecisionSubstantially Equivalent, May 19, 1978
ReceivedApr 25, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780702

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.