510(k) K163135 ยท DQA Oximeter
Finger Pulse Oximeter
| Applicant | Shenzhen Fitfaith Technology Co.,Ltd, Guangming New District, Shenzhen, CN |
| Decision | Substantially Equivalent, Sep 19, 2017 |
| Received | Nov 8, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163135
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.