ClearanceBrief
510(k) K220117 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

ARC Intensive Care Information System (ARC System)

ApplicantOrdinatrum Solutions, Tustin CA, US
DecisionSubstantially Equivalent, Jun 6, 2023
ReceivedJan 14, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220117

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.