510(k) K161938 ยท DQA Oximeter
Fingertip Pulse Oximeter
| Applicant | Xuzhou Yongkang Electronic Science Technology Co., Ltd., Xuzhou, CN |
| Decision | Substantially Equivalent, May 8, 2017 |
| Received | Jul 14, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161938
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.