510(k) K151024 ยท DQA Oximeter
Finger Type Pulse Oximeter
| Applicant | Taidoc Technology Corporation, New Taipei City, TW |
| Decision | Substantially Equivalent, Mar 2, 2016 |
| Received | Apr 16, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151024
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.