510(k) K030108 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
ARTHROCARE ENT COBLATOR SURGERY SYSTEM
| Applicant | Arthrocare Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Feb 3, 2003 |
| Received | Jan 13, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030108
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 26, 2015 | ArthroCare Medical Corporation Coblator II System, 120V.
Product Usage: The Coblator II (Model RF8000E) is a bipolar, radiofrequency electrosurgical system designed for use in otorhinolaryngology (ENT) surgery. The system consis Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.