510(k) K200856 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
SmartLinx Vitals Plus Patient Monitoring System
| Applicant | Capsule Technologie Sas, Andover MA, US |
| Decision | Substantially Equivalent, Jul 10, 2020 |
| Received | Apr 1, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200856
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.