510(k) K021829 ยท MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
MODIFICATION TO KODAK DIRECTVIEW CR 800/900 SYSTEM
| Applicant | Eastman Kodak Company, Rochester NY, US |
| Decision | Substantially Equivalent, Jul 2, 2002 |
| Received | Jun 4, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021829
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.