510(k) K011917 ยท KGI Densitometer, Bone
ADVANCED HIP ASSESSMENT SOFTWARE
| Applicant | Ge Lunar Corp., Madison WI, US |
| Decision | Substantially Equivalent, Aug 3, 2001 |
| Received | Jun 20, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011917
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.