Company ยท US
Capsule Technologie
FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2021. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| MWI | Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | 9 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 19, 2021 | K210204 | Capsule Vitals Plus Patient Monitoring System Capsule Technologie Sas, FR | MWI |
| Jul 10, 2020 | K200856 | SmartLinx Vitals Plus Patient Monitoring System Capsule Technologie Sas | MWI |
| Apr 17, 2019 | K183638 | SmartLinx Vitals Plus Patient Monitoring System Capsule Technologie | MWI |
| Aug 8, 2018 | K180734 | SmartLinx Vitals Plus Patient Monitoring System Capsule Technologie | MWI |
| Oct 24, 2017 | K171751 | SmartLinx Vitals Plus NIBP Module, SmartLinx Vitals Plus License for Spot Monitoring Mode, SmartLinx Vitals Plus Alarm H Capsule Technologie Sas | MWI |
| Sep 17, 2015 | K151071 | SmartLinx Vitals Plus Patient Monitoring System Capsule Technologie Sas | MWI |
| Aug 8, 2003 | K032142 | DATACAPTOR Capsule Technologie | MWI |
| Feb 21, 2002 | K020197 | MODIFICATION TO DATACAPTOR Capsule Technologie | MWI |
| Dec 18, 2001 | K013019 | DATACAPTOR Capsule Technologie | MWI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||