510(k) K093596 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic
LUMOS, MODEL R 72B
| Applicant | Lumos, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jan 12, 2010 |
| Received | Nov 20, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093596
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.