510(k) K011111 ยท KPR System, X-Ray, Stationary
MXD100/MX 20, OR MX 30, OR MX 40 OR MX 50--(MXD 100 SERIES)
| Applicant | Modular X-Ray Devices, Roodepoort, ZA |
| Decision | Substantially Equivalent, May 30, 2001 |
| Received | Apr 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011111
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.