510(k) K023554 ยท KGI Densitometer, Bone
DUAL-ENERGY VERTEBRAL ASSESSMENT VIEW SOFTWARE
| Applicant | Ge Lunar Corp., Madison WI, US |
| Decision | Substantially Equivalent, Dec 20, 2002 |
| Received | Oct 23, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023554
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.