510(k) K913321 ยท KGI Densitometer, Bone
HOLOGIC QDR-2000 X-RAY BONE DENSITOMETER
| Applicant | Hologic, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Nov 1, 1991 |
| Received | Jul 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913321
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.