510(k) K033377 ยท LMC Camera, Multi Format, Radiological
FUJI MEDICAL DRY LASER IMAGERS, MODELS DRYPIX 7000, DRYPIX 5000 AND FM-DP L
| Applicant | Fujifilm Medical System U.S.A., Inc., Stamford CT, US |
| Decision | Substantially Equivalent, Jan 9, 2004 |
| Received | Oct 22, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033377
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.