ClearanceBrief
510(k) K770245 ยท KXN Monitor, Cardiac, Fetal

ABDOMINAL FETAL ECG MODULE

ApplicantMennen Greatbatch Electonics, Mchenry IL, US
DecisionSubstantially Equivalent, Feb 14, 1977
ReceivedFeb 7, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770245

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.