ClearanceBrief
510(k) K113165 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

MINI-MEDIC

ApplicantAthena Gtx, Des Moines IA, US
DecisionSubstantially Equivalent, Feb 2, 2012
ReceivedOct 26, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113165

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.