510(k) K905071 ยท EKX Handpiece, Direct Drive, Ac-Powered
MX CYCLER
| Applicant | Dakmed, Inc., Buffalo NY, US |
| Decision | Substantially Equivalent, May 28, 1991 |
| Received | Nov 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905071
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.