ClearanceBrief
510(k) K191989 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

WVSM (Wireless Vital Signs Monitor) RWC + miniCap

ApplicantAthena Gtx, Johnson IA, US
DecisionSubstantially Equivalent, Jan 29, 2020
ReceivedJul 25, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K191989

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.