510(k) K904980 ยท KGI Densitometer, Bone
DPX-L AND DPX-ALPHA, MODIFICATION
| Applicant | Lunar, Madison WI, US |
| Decision | Substantially Equivalent, Dec 5, 1990 |
| Received | Nov 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904980
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.