510(k) K070374 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
ARTHROCARE ENT PLASMA WAND
| Applicant | Arthrocare Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Apr 25, 2007 |
| Received | Feb 8, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070374
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 18, 2015 | ArthroCare Corporation EVac 70 XTRA with Integrated Cable and PROcise EZ View with Integrated Cable
Product Usage:
PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.