ClearanceBrief
510(k) K141811 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

MORTARA MONITORING WAVEFORM VIEWER

ApplicantMortara Instrument, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Nov 19, 2014
ReceivedJul 7, 2014
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K141811

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.