510(k) K103265 ยท KGI Densitometer, Bone
NHANES WHOLE BODY DXA REFERENCE DATABASE
| Applicant | Hologic, Inc., Bedford MA, US |
| Decision | Substantially Equivalent, Mar 16, 2011 |
| Received | Nov 4, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103265
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.