510(k) K042480 ยท KGI Densitometer, Bone
INFANT WHOLE BODY SOFTWARE OPTION FOR QDR DENSITOMETERS
| Applicant | Hologic, Inc., Bedford MA, US |
| Decision | Substantially Equivalent, Oct 29, 2004 |
| Received | Sep 13, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042480
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.