ClearanceBrief
510(k) K821942 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

HARVEY-BOSTWICK BRADY CARDIA MONIT. HB85

ApplicantHarvey-Bostwick, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 24, 1982
ReceivedJun 29, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821942

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.