510(k) K980809 ยท LMA Digitizer, Image, Radiological
LUMISCAN 135 PHOSPHOR PLATE DIGITIZER/LUMISYS 135 ERASER
| Applicant | Lumisys, Inc., San Leandro CA, US |
| Decision | Substantially Equivalent, May 11, 1998 |
| Received | Mar 3, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980809
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.