510(k) K992775 ยท KGI Densitometer, Bone
OPTION FOR THE QDR BONE DENSITOMETER, MODELS QDR4500, QDR2000, QDR1500, QDR4000, QDR1000, QDR1000W
| Applicant | Hologic, Inc., Bedford MA, US |
| Decision | Substantially Equivalent, Oct 1, 1999 |
| Received | Aug 18, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992775
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.