510(k) K001756 ยท KGI Densitometer, Bone
LUNAR REPORT GENERATOR II
| Applicant | Lunar Corp., Madison WI, US |
| Decision | Substantially Equivalent, Jul 6, 2000 |
| Received | Jun 9, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001756
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.