ClearanceBrief
510(k) K030466 ยท KNG Monitor, Ultrasonic, Fetal

HANDYDOP

ApplicantElcat, GmbH, Alpharetta GA, US
DecisionSubstantially Equivalent, Sep 12, 2003
ReceivedFeb 12, 2003
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K030466

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.