510(k) K984178 ยท KGI Densitometer, Bone
PRONOSCO X-POSURE SYSTEM
| Applicant | Torsana Osteoporosis Diagnostics A/S, Washington DC, US |
| Decision | Substantially Equivalent, Feb 18, 1999 |
| Received | Nov 20, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984178
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.