ClearanceBrief
510(k) K781360 ยท HGM System, Monitoring, Perinatal

MODEL 80100A, PATIENT DATA MEMORY

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 7, 1978
ReceivedAug 7, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781360

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.