510(k) K883280 ยท KGI Densitometer, Bone
HOLOGIC QDR-1000 X-RAY BONE DENSITOMETER/MODIFIED
| Applicant | Hologic, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Sep 29, 1988 |
| Received | Aug 3, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883280
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.