510(k) K230914 · GEI Electrosurgical, Cutting & Coagulation & Accessories
ARIS¿ COBLATION¿ Turbinate Reduction Wand (72290113); WEREWOLF COBLATION System (72290144); WEREWOLF+ COBLATION System (72290146)
| Applicant | ArthroCare Corporation, Austin TX, US |
| Decision | Substantially Equivalent, Jun 26, 2023 |
| Received | Mar 31, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230914
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.