510(k) K980125 ยท KGI Densitometer, Bone
REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER
| Applicant | Norland Corp., Fort Atkinson WI, US |
| Decision | Substantially Equivalent, May 20, 1998 |
| Received | Jan 14, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980125
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.