ClearanceBrief
510(k) K895909 ยท MAA Monitor, Fetal Doppler Ultrasound

SONICAID MODEL VASOFLO 4

ApplicantOxford Medilog, Inc., Clearwater FL, US
DecisionSubstantially Equivalent, Jul 9, 1990
ReceivedOct 10, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895909

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.