ClearanceBrief
510(k) K930004 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

ESCORT 100/300 SERIES B PATIENT MONITORS

ApplicantMedical Data Electronics, Arleta CA, US
DecisionSubstantially Equivalent, Jun 23, 1993
ReceivedJan 4, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930004

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.