ClearanceBrief
510(k) K152701 ยท DSI Detector And Alarm, Arrhythmia

Matrix Mini ECG Monitor

ApplicantGlobal Instrumentation, LLC, Manlius NY, US
DecisionSubstantially Equivalent, Apr 22, 2016
ReceivedSep 21, 2015
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K152701

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.