510(k) K163382 ยท DQA Oximeter
Oxitone 1000
| Applicant | Oxitone Medical , Ltd., Kfar Saba, IL |
| Decision | Substantially Equivalent, May 9, 2017 |
| Received | Dec 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163382
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.