510(k) K180953 ยท EKX Handpiece, Direct Drive, Ac-Powered
AnyCheck IMT-100
| Applicant | Dms Co., Ltd., Wonju-Si, KR |
| Decision | Substantially Equivalent, Feb 20, 2019 |
| Received | Apr 11, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180953
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.