510(k) K210423 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Werewolf+ Coblation System, Werewolf+ Controller, Werewolf Fastseal 6.0 Hemostasis Wand
| Applicant | ArthroCare Corporation, Austin TX, US |
| Decision | Substantially Equivalent, Jun 24, 2021 |
| Received | Feb 11, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210423
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.