ClearanceBrief
510(k) K942887 ยท HGM System, Monitoring, Perinatal

MODEL M1310A, SERIES 50T FETAL TELEMETRY SYSTEM

ApplicantHewlett-Packard Co., Waltham MA, US
DecisionSubstantially Equivalent, Aug 15, 1994
ReceivedJun 20, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942887

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.