510(k) K960834 ยท IYE Accelerator, Linear, Medical
KODAK EC-L CASSETTE
| Applicant | Eastman Kodak Company, Rochester NY, US |
| Decision | Substantially Equivalent, May 28, 1996 |
| Received | Feb 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960834
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.