510(k) K180734 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, Aug 8, 2018 |
| Received | Mar 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180734
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.