ClearanceBrief
510(k) K212143 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

Neteera 130H/131H Vital Sign Monitoring Sensor

ApplicantNeteera Technologies , Ltd., Jerusalem, IL
DecisionSubstantially Equivalent, Sep 28, 2022
ReceivedJul 9, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212143

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.