510(k) K905291 ยท KGI Densitometer, Bone
LATERAL SPINE DETERMAINATIONS DPX/DPX-L/DPX-ALPHA
| Applicant | Lunar, Madison WI, US |
| Decision | Substantially Equivalent, Aug 9, 1991 |
| Received | Nov 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905291
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.