510(k) K210204 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Capsule Vitals Plus Patient Monitoring System
| Applicant | Capsule Technologie Sas, Paris, FR |
| Decision | Substantially Equivalent, Oct 19, 2021 |
| Received | Jan 26, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210204
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.