510(k) K003714 ยท EKX Handpiece, Direct Drive, Ac-Powered
OSSTELL RESONANCE FREQUENCY ANALYZER
| Applicant | Integration Diagnostics, Ltd., Findley MN, US |
| Decision | Substantially Equivalent, Aug 9, 2001 |
| Received | Dec 1, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003714
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.