510(k) K193350 ยท DQA Oximeter
Leadtek Fingertip Pulse Oximeter
| Applicant | Leadtek Research, Inc., New Taipei City, TW |
| Decision | Substantially Equivalent, Apr 27, 2020 |
| Received | Dec 3, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193350
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.