510(k) K030487 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic
R 72
| Applicant | Ralco S.R.L., Deerfield IL, US |
| Decision | Substantially Equivalent, Aug 1, 2003 |
| Received | Feb 14, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030487
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.