510(k) K092675 ยท HCC Device, Biofeedback
GRINDCARE
| Applicant | Medotech A/S, Westminster CO, US |
| Decision | Substantially Equivalent, Mar 3, 2010 |
| Received | Sep 1, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092675
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.