510(k) K122298 ยท IZL System, X-Ray, Mobile
AJEX 1200 H / AJEX 240H MOBILE X-RAY GENERATOR
| Applicant | Ajex Meditech., Ltd., Plainview NY, US |
| Decision | Substantially Equivalent, Mar 28, 2014 |
| Received | Jul 31, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122298
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.