510(k) K946320 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic
R 302
| Applicant | Ralco S.R.L., Italy, IT |
| Decision | Substantially Equivalent, May 11, 1995 |
| Received | Dec 28, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K946320
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.