510(k) K802180 ยท KGI Densitometer, Bone
WISCONSIN DUAL-PHOTON BONE ANALYZER
| Applicant | Lunar Radiation Corp. WI, US |
| Decision | Substantially Equivalent, Dec 31, 1980 |
| Received | Sep 9, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802180
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.