510(k) K984285 ยท KGI Densitometer, Bone
OSTEOGRAM BONE DENSITOMETER
| Applicant | Compumed, Inc., Rockville MD, US |
| Decision | Substantially Equivalent, May 19, 1999 |
| Received | Dec 1, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984285
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.