Capsule Technologie Sas
Capsule Technologie Sas holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2021.
Top product codes for Capsule Technologie Sas
Recent clearances by Capsule Technologie Sas
- K210204 — Capsule Vitals Plus Patient Monitoring System
- K200856 — SmartLinx Vitals Plus Patient Monitoring System
- 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 Module
- K151071 — SmartLinx Vitals Plus Patient Monitoring System
Data sourced from openFDA. This site is unofficial and independent of the FDA.