510(k) K973459 ยท KGI Densitometer, Bone
NORLAND BODY COMPOSITION OPTION FOR NORLAND DEXA BONE DENSITOMETERS
| Applicant | Norland Corp., Fort Atkinson WI, US |
| Decision | Substantially Equivalent, Feb 13, 1998 |
| Received | Sep 12, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973459
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.