510(k) K961787 ยท KGI Densitometer, Bone
BODY COMPOSITION SOFTWARE OPTION FOR QDR X-RAY BONE DENSITOMETERS
| Applicant | Hologic, Inc., Rockville MD, US |
| Decision | Substantially Equivalent, Jun 13, 1997 |
| Received | May 9, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961787
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.