ClearanceBrief
510(k) K122133 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING

ApplicantAirstrip Technologies, LP, San Antonio TX, US
DecisionSubstantially Equivalent, Oct 2, 2012
ReceivedJul 18, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K122133

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.