510(k) K011827 ยท KQX Goniometer, Ac-Powered
ORTELIUS 800
| Applicant | Orthoscan , Ltd., Ra'Ananna, IL |
| Decision | Substantially Equivalent, Aug 28, 2001 |
| Received | Jun 12, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011827
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.