ClearanceBrief
510(k) K831371 ยท HGM System, Monitoring, Perinatal

MODEL FM5

ApplicantSonicaid, Inc., Walker MI, US
DecisionSubstantially Equivalent, Jun 30, 1983
ReceivedApr 27, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831371

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.