510(k) K961011 ยท KGI Densitometer, Bone
DTX-200 BONE DENSITOMETER
| Applicant | Shotwell & Carr, Inc., Dallas TX, US |
| Decision | Substantially Equivalent, Jul 5, 1996 |
| Received | Mar 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961011
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.