510(k) K202006 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
ENT Plasma Wands, Turbinator Wand, Werewolf Irrigation Tube Set, Werewolf ENT Adapter, Werewolf Coblation System
| Applicant | ArthroCare Corporation, Austin TX, US |
| Decision | Substantially Equivalent, Dec 18, 2020 |
| Received | Jul 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202006
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.