510(k) K221979 ยท DQA Oximeter
Pulse Oximeter (Model C101A2, C101B1, C101A3)
| Applicant | Shenzhen Imdk Medical Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Oct 16, 2022 |
| Received | Jul 5, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K221979
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.