510(k) K082604 ยท KPR System, X-Ray, Stationary
VIZTEK DR, MODELS: DR1000, DR3000, DR4000
| Applicant | Viztek, Inc., Deer Field IL, US |
| Decision | Substantially Equivalent, Nov 21, 2008 |
| Received | Sep 8, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082604
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.