510(k) K961007 ยท KGI Densitometer, Bone
EXPERT SPINE MORPHOTIETRY REFERENCE
| Applicant | Lunar Corp., Madison WI, US |
| Decision | Substantially Equivalent, Jul 25, 1996 |
| Received | Mar 12, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961007
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.