510(k) K884625 ยท KGI Densitometer, Bone
DPX BONE DENSITOMETER FOR TOTAL BODY BONE DENSITY
| Applicant | Lunar, Madison WI, US |
| Decision | Substantially Equivalent, Jun 23, 1989 |
| Received | Nov 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884625
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.