ClearanceBrief
510(k) K040819 ยท HGM System, Monitoring, Perinatal

TRANSDUCER FOR ULTRASOUND FETAL MONITORING, MODELS FM10833 AND FM10834

ApplicantAmerican I.V. Products, Inc., Hanover MD, US
DecisionSubstantially Equivalent, Aug 16, 2004
ReceivedMar 30, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040819

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.