ClearanceBrief
510(k) K895763 ยท KXO Monitor, Pressure, Intrauterine

ISOFLO AND ISOTEC INTRAUTERINE PRESSURE MONITORING

ApplicantHealthdyne Cardiovascular, Inc., Costa Mesa CA, US
DecisionSubstantially Equivalent, Dec 22, 1989
ReceivedSep 26, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895763

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.