510(k) K160268 ยท DQA Oximeter
Fingertip Pulse Oximeter MD300CG11/MD300CG51
| Applicant | Beijing Choice Electronic Technology Co., Ltd., Beijing, CN |
| Decision | Substantially Equivalent, Oct 14, 2016 |
| Received | Feb 2, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160268
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.