510(k) K173045 ยท DQA Oximeter
Oximeter
| Applicant | Shenzhen Greatmade Tech Limited, Shenzhen, CN |
| Decision | Substantially Equivalent, Jun 5, 2018 |
| Received | Sep 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173045
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.