510(k) K960839 ยท LMA Digitizer, Image, Radiological
FILM SCANNER 300
| Applicant | Cannon U.S.A., Inc., Lake Success NY, US |
| Decision | Substantially Equivalent, Dec 18, 1996 |
| Received | Feb 26, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960839
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.