510(k) K813348 ยท EKX Handpiece, Direct Drive, Ac-Powered
YOSHIDA RIDO-F, MODEL LM-01
| Applicant | Kaycor Intl., Ltd., Walker MI, US |
| Decision | Substantially Equivalent, Jan 7, 1982 |
| Received | Nov 27, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813348
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.