510(k) K953032 ยท KGI Densitometer, Bone
LUNAR DPX DENSITOMETER
| Applicant | Lunar Corp., Madison WI, US |
| Decision | Substantially Equivalent, Oct 23, 1995 |
| Received | Jun 30, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953032
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.