ClearanceBrief
510(k) K984033 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

ATLAS MONITOR

ApplicantWelch Allyn, Inc., Skaneateles Falls NY, US
DecisionSubstantially Equivalent, Jul 8, 1999
ReceivedNov 12, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K984033

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.