510(k) K170965 ยท DQA Oximeter
Fingertip Pulse Oximeter
| Applicant | Shenzhen Jumper Medical Equipment Co., Ltd., Baoan District, Shenzhen, CN |
| Decision | Substantially Equivalent, Nov 3, 2017 |
| Received | Mar 31, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170965
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.