510(k) K183638 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
SmartLinx Vitals Plus Patient Monitoring System
| Applicant | Capsule Technologie, Andover MA, US |
| Decision | Substantially Equivalent, Apr 17, 2019 |
| Received | Dec 26, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K183638
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.