510(k) K142999 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
EVac 70 Xtra Plasma Wand with Integrated Cable, PROcise XP Plasma Wand with Integrated Cable
| Applicant | ArthroCare Corporation, Austin TX, US |
| Decision | Substantially Equivalent, Nov 19, 2014 |
| Received | Oct 17, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K142999
| 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 |
| Jun 25, 2015 | ArthroCare Medical Corporation EVAC 70 XTRA with Integrated Cable REF EICA5872-01
Product Usage:
PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in otorhino Terminated |
GEI | None listed |
| Jun 25, 2015 | ArthroCare Medical Corporation PROcise XP Wand with Integrated Cable REF EICA8872-01
Product Usage:
PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in otorh Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.