510(k) K904489 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic
EUREKA EXTENSION CYLINDERS
| Applicant | Eureka X-Ray Tube Corp., Arlington Heights IL, US |
| Decision | Substantially Equivalent, Oct 15, 1990 |
| Received | Oct 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904489
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.