510(k) K002711 ยท KGI Densitometer, Bone
HOLOGIC QDR X-RAY BONE DENSITOMETER/MODELS SERIES 4500, 4000, 2000, 1000 AND HOLOGIC DELPHI X-RAY BONE DENSITOMETER
| Applicant | Hologic, Inc., Bedford MA, US |
| Decision | Substantially Equivalent, Sep 28, 2000 |
| Received | Aug 31, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002711
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.