510(k) K150869 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Checkme Pro Health Monitor
| Applicant | Viatom Technology Co., Ltd., Nanshan, Shenzhen, CN |
| Decision | Substantially Equivalent, Dec 10, 2015 |
| Received | Apr 1, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150869
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.