510(k) K210032 ยท DQA Oximeter
Leadtek Fingertip Pulse Oximeter (Wireless), Leadtek Fingertip Pulse Oximeter (Wireless)
| Applicant | Leadtek Research, Inc., New Taipei City, TW |
| Decision | Substantially Equivalent, Sep 1, 2021 |
| Received | Jan 5, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K210032
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.