ClearanceBrief
510(k) K010587 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

ACTIVEECG

ApplicantActive Corp., Castine ME, US
DecisionSubstantially Equivalent, May 16, 2001
ReceivedFeb 27, 2001
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K010587

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.