510(k) K172965 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Handheld VitalSigns Monitoring System
| Applicant | Visiomed Technology Co.,Ltd, Bao An, Shenzhen,, CN |
| Decision | Substantially Equivalent, Dec 17, 2018 |
| Received | Sep 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172965
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.