510(k) K091752 ยท KPR System, X-Ray, Stationary
VIZTEK WL
| Applicant | Viztek, Inc., Deer Field IL, US |
| Decision | Substantially Equivalent, Nov 12, 2009 |
| Received | Jun 16, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091752
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.