ClearanceBrief
510(k) K191110 · KNG Monitor, Ultrasonic, Fetal

HeraBEAT™ US

ApplicantHeramed, Ltd., Netanya, IL
DecisionSubstantially Equivalent, Nov 14, 2019
ReceivedApr 26, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K191110

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.