510(k) K890999 ยท KGI Densitometer, Bone
MODIFIED QDR-1000 X-RAY BONE DENSITOMETER
| Applicant | Hologic, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Dec 21, 1989 |
| Received | Feb 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890999
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.