510(k) K191088 ยท DQA Oximeter
Checkme O2 Pulse Oximeter
| Applicant | Shenzhen Viatom Technology Co., Ltd., Baoan District Guandong, CN |
| Decision | Substantially Equivalent, Dec 2, 2019 |
| Received | Apr 24, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191088
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.