510(k) K964562 ยท KGI Densitometer, Bone
DTX-200 BONE DENSITOMETER
| Applicant | Osteometer Meditech A/S, Dallas TX, US |
| Decision | Substantially Equivalent, Aug 22, 1997 |
| Received | Nov 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964562
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.