ClearanceBrief
510(k) K830666 ยท DPS Electrocardiograph

APNEA/BRADYCARDIA MONITOR HB 95

ApplicantHarvey-Bostwick, Inc., Walker MI, US
DecisionSubstantially Equivalent, Jul 18, 1983
ReceivedMar 4, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830666

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.