510(k) K220871 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
Nautilus
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Apr 18, 2022 |
| Received | Mar 25, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K220871
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.