510(k) K832063 ยท EKX Handpiece, Direct Drive, Ac-Powered
ROBIN CORDLESS HANDPIECE
| Applicant | Kaycor Intl., Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 26, 1983 |
| Received | Jun 27, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832063
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.