510(k) K162770 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Relign System
| Applicant | Relign Corporation, Cupertino CA, US |
| Decision | Substantially Equivalent, Jan 4, 2017 |
| Received | Oct 3, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162770
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.