Capsule Technologie Sas - FDA 510(k) Cleared Devices
Recent clearances: Capsule Vitals Plus Patient Monitoring System, SmartLinx Vitals Plus Patient Monitoring System
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Capsule Technologie Sas Cardiovascular ✕
4 devices
Cleared
Oct 19, 2021
Capsule Vitals Plus Patient Monitoring System
Cardiovascular
266d
Cleared
Jul 10, 2020
SmartLinx Vitals Plus Patient Monitoring System
Cardiovascular
100d
Cleared
Oct 24, 2017
SmartLinx Vitals Plus NIBP Module, SmartLinx Vitals Plus License for Spot...
Cardiovascular
133d
Cleared
Sep 17, 2015
SmartLinx Vitals Plus Patient Monitoring System
Cardiovascular
149d