510(k) K843922 ยท KGI Densitometer, Bone
OSTEON BONE MINERAL ANALYZER
| Applicant | Osteon, Inc., Wahiawa HI, US |
| Decision | Substantially Equivalent, Apr 2, 1985 |
| Received | Oct 5, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843922
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.