510(k) K974437 ยท KGI Densitometer, Bone
EXPERT-XL LATERAL SPINE BMD ACQUISITION AND ANALYSIS SOFTWARE
| Applicant | Lunar Corp., Madison WI, US |
| Decision | Substantially Equivalent, Feb 13, 1998 |
| Received | Nov 24, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974437
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.