510(k) K002500 ยท KGI Densitometer, Bone
X-POSURE SYSTEM VERSION 2 RAD
| Applicant | Pronosco A/S, Washington DC, US |
| Decision | Substantially Equivalent, Oct 23, 2000 |
| Received | Aug 14, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002500
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.