ClearanceBrief
510(k) K800500 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

PULSEOMETER

ApplicantKirklands Sporting Goods Co., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 8, 1980
ReceivedMar 4, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800500

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.