510(k) K003656 ยท KGI Densitometer, Bone
X-POSURE SYSTEM VERSION 2 MAMMO
| Applicant | Pronosco A/S, Washington DC, US |
| Decision | Substantially Equivalent, Dec 15, 2000 |
| Received | Nov 27, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K003656
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.