ClearanceBrief
510(k) K100155 ยท DSI Detector And Alarm, Arrhythmia

TRUVUE WIRELESS AMBULATORY ECG MONITORING SYSTEM

ApplicantBiomedical Systems Corp., St. Louis MO, US
DecisionSubstantially Equivalent, Apr 20, 2010
ReceivedJan 20, 2010
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K100155

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.