ClearanceBrief
510(k) K850113 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

C/PES 9103, ECG STRESS TESTING SYSTEM

ApplicantGould, Inc., Dayton OH, US
DecisionSubstantially Equivalent, Feb 8, 1985
ReceivedJan 14, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850113

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.