510(k) K980569 ยท KGI Densitometer, Bone
FRACTURE RISK ASSESSMENT CAPABILITY FOR NORLAND X-RAY BONE DENSITOMETERS
| Applicant | Norland Corp., Fort Atkinson WI, US |
| Decision | Substantially Equivalent, Jun 12, 1998 |
| Received | Feb 13, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980569
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.