510(k) K033821 ยท LMC Camera, Multi Format, Radiological
KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY
| Applicant | Eastman Kodak Company, Oakdale MN, US |
| Decision | Substantially Equivalent, Feb 20, 2004 |
| Received | Dec 9, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033821
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.