510(k) K171829 ยท OWB Interventional Fluoroscopic X-Ray System
EndoNaut
| Applicant | Therenva Sas, Rennes, FR |
| Decision | Substantially Equivalent, Sep 21, 2017 |
| Received | Jun 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171829
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.