510(k) K970293 ยท LMD System, Digital Image Communications, Radiological
FUJI COMPUTED RADIOGRAPHY FCR/DICOM GATEWAY UNIT CR-DM666
| Applicant | Fujifilm Medical System U.S.A., Inc., Stamford CT, US |
| Decision | Substantially Equivalent, Mar 21, 1997 |
| Received | Jan 24, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970293
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.