ClearanceBrief
510(k) K090696 ยท QYX Outpatient Cardiac Telemetry

NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEM

ApplicantCorventis, Inc., San Jose CA, US
DecisionSubstantially Equivalent, Jun 19, 2009
ReceivedMar 16, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K090696

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.