510(k) K102123 ยท KPR System, X-Ray, Stationary
VIZION DR
| Applicant | Viztek, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jan 24, 2011 |
| Received | Jul 29, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102123
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.