510(k) K033224 ยท KGI Densitometer, Bone
HOLOGIC QDR EXPLORER X-RAY BONE DENSITOMETER, MODEL EXPLORER
| Applicant | Hologic, Inc., Bedford MA, US |
| Decision | Substantially Equivalent, Nov 5, 2003 |
| Received | Oct 6, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033224
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.