510(k) K023398 ยท KGI Densitometer, Bone
HOLOGIC QDR X-RAY BONE DENSITOMETER, MODELS 1000, 2000, 4500, DELPHI, DISCOVERY
| Applicant | Hologic, Inc., Bedford MA, US |
| Decision | Substantially Equivalent, Nov 8, 2002 |
| Received | Oct 9, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023398
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 16, 2024 | Hologic Inc Horizon X-Ray Bone Densitometer (DXA)
Models: Horizon-A, Horizon-W, Horizon-WI, Horizon-C, Horizon-CI, Horizon-A-CN, Horizon-W-CN, Horizon-WI-CN, Horizon-CI-CN Open, Classified |
KGI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.