510(k) K122768 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
GENESIS
| Applicant | Dornier Medtech America, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jan 18, 2013 |
| Received | Sep 10, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122768
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.