510(k) K062788 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic
COLLIMATOR, MODEL M-38
| Applicant | Umi International, Norwood NJ, US |
| Decision | Substantially Equivalent, Dec 28, 2006 |
| Received | Sep 18, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062788
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.