510(k) K963789 ยท KGI Densitometer, Bone
DTX-100 BONE DENSITOMETER
| Applicant | Osteometer Meditech A/S, Dallas TX, US |
| Decision | Substantially Equivalent, Jul 14, 1997 |
| Received | Sep 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963789
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.