ClearanceBrief
510(k) K902690 ยท HGM System, Monitoring, Perinatal

SONICAID MODEL MERIDIAN 800

ApplicantOxford Medilog, Inc., Clearwater FL, US
DecisionSubstantially Equivalent, Feb 5, 1991
ReceivedJun 19, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902690

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.