510(k) K983028 ยท KGI Densitometer, Bone
FRACTURE RISK OPTION FOR THE QDR BONE DENSITOMETER, MODEL#S QDR4500, QDR2000, QDR1500, QDR4000, QDR1000, QDR1000W
| Applicant | Hologic, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Nov 13, 1998 |
| Received | Aug 31, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983028
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.