ClearanceBrief
510(k) K801747 ยท HGM System, Monitoring, Perinatal

TERUMO FETAL MONITOR # FHM-602

ApplicantTerumo Medical Corp., Elkton MD, US
DecisionSubstantially Equivalent, Aug 13, 1980
ReceivedJul 28, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801747

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.