510(k) K033689 ยท EKX Handpiece, Direct Drive, Ac-Powered
OSSTELL MENTOR RFA
| Applicant | Integration Diagnostics, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Feb 26, 2004 |
| Received | Nov 24, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033689
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.