510(k) K960326 ยท LMB Device, Digital Image Storage, Radiological
FCR DMS OPTICAL DISK IMAGE FILING UNIT OD-F614, ODF614L & MULTIMODALITY SYSTEM
| Applicant | Fujifilm Medical System U.S.A., Inc., Stamford CT, US |
| Decision | Substantially Equivalent, Mar 7, 1996 |
| Received | Jan 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960326
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.