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Capsule Technologie Sas

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories1
Latest FDA decision2021-10-19
TypeNumberDevice NameCodeDateActions
510(k) K210204 Capsule Vitals Plus Patient Monitoring SystemMWI2021-10-19 View
510(k) K200856 SmartLinx Vitals Plus Patient Monitoring SystemMWI2020-07-10 View
510(k) K171751 SmartLinx Vitals Plus NIBP Module, SmartLinx Vitals Plus License for Spot Monitoring Mode, SmartLinx Vitals Plus Alarm Hub, SmartLinx Vitals Plus License for Advanced Monitoring Mode, Covidien FILAC 3000 - Temperature ModuleMWI2017-10-24 View
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