ClearanceBrief
510(k) K921957 ยท HGM System, Monitoring, Perinatal

HEWLETT-PACKARD MODEL M1351A FETAL MONITOR

ApplicantHewlett-Packard Co., Germany, DE
DecisionSubstantially Equivalent, Sep 24, 1993
ReceivedApr 27, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921957

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.