510(k) K172805 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
gi-4000 Electrosurgical Generator
| Applicant | United States Endoscopy Group, Inc., Mentor OH, US |
| Decision | Substantially Equivalent, Oct 23, 2017 |
| Received | Sep 18, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K172805
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.