510(k) K162074 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Werewolf RF20000 Controller, FLOW 50 Wand
| Applicant | ArthroCare Corporation, Austin TX, US |
| Decision | Substantially Equivalent, Aug 22, 2016 |
| Received | Jul 27, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162074
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.