510(k) K060111 ยท KGI Densitometer, Bone
IVA (MXA II SOFTWARE OPTION)
| Applicant | Hologic, Inc., Bedford MA, US |
| Decision | Substantially Equivalent, Apr 24, 2006 |
| Received | Jan 17, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060111
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.