510(k) K963363 ยท KGI Densitometer, Bone
HOLOGIC QDR SERIES X-RAY BOE DENSITOMETERS
| Applicant | Hologic, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Nov 22, 1996 |
| Received | Aug 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963363
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.