510(k) K082402 ยท KGI Densitometer, Bone
OSDX HIP BMD SYSTEM
| Applicant | Imaging Therapeutics, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Oct 16, 2008 |
| Received | Aug 20, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082402
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.