510(k) K964307 ยท KGI Densitometer, Bone
EXPANDED REFERENCE VALUES FOR DPX BON DENSITOMETERS
| Applicant | Lunar Corp., Madison WI, US |
| Decision | Substantially Equivalent, Apr 16, 1997 |
| Received | Oct 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964307
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.