K120418 is an FDA 510(k) clearance for the ELECTROSUGRICAL RESECTION AND VAPORIZATION ELECTRODE SERIES. This device is classified as a Electrode, Electrosurgical, Active, Urological (Class II - Special Controls, product code FAS).
Submitted by Olympus Winter & Ibe GmbH (Center Valley, US). The FDA issued a Cleared decision on June 20, 2012, 131 days after receiving the submission on February 10, 2012.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.4300.
| 510(k) Number | K120418 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 10, 2012 |
| Decision Date | June 20, 2012 |
| Days to Decision | 131 days |
| Submission Type | Special |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FAS — Electrode, Electrosurgical, Active, Urological |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.4300 |