510(k) K082317 ยท KGI Densitometer, Bone
GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTION
| Applicant | General Electric Co., Madison WI, US |
| Decision | Substantially Equivalent, Sep 26, 2008 |
| Received | Aug 13, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082317
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.