510(k) K212043 ยท EKX Handpiece, Direct Drive, Ac-Powered
TRAUS ENDO
| Applicant | Saeshin Precision Co., Ltd., Daegu, KR |
| Decision | Substantially Equivalent, Jun 24, 2022 |
| Received | Jun 30, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K212043
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.