ClearanceBrief
510(k) K091971 ยท DSI Detector And Alarm, Arrhythmia

AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEM

ApplicantCorventis, Inc., San Jose CA, US
DecisionSubstantially Equivalent, Aug 27, 2009
ReceivedJul 1, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K091971

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.