510(k) K063007 ยท EKX Handpiece, Direct Drive, Ac-Powered
POWERTOME PERIOTOME
| Applicant | Westport Medical, Inc., Salem OR, US |
| Decision | Substantially Equivalent, Oct 17, 2006 |
| Received | Oct 2, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063007
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.