510(k) K933408 ยท IXW Processor, Radiographic-Film, Automatic
FUJI DAYLIGHT CASSETTE MULTI-LOADER
| Applicant | Fujifilm Medical System U.S.A., Inc., Stamford CT, US |
| Decision | Substantially Equivalent, Aug 16, 1993 |
| Received | Jul 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933408
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.