K981256 is an FDA 510(k) clearance for the ISOLATED SALINE ELECTRODES/PROBES/DEVICES-SALINETRODE. This device is classified as a Electrode, Electrosurgical, Active, Urological (Class II - Special Controls, product code FAS).
Submitted by Ximed/Prosure/Injectx (San Jose, US). The FDA issued a Cleared decision on May 12, 1998, 40 days after receiving the submission on April 2, 1998.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.4300.
| 510(k) Number | K981256 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 02, 1998 |
| Decision Date | May 12, 1998 |
| Days to Decision | 40 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Statement |
| Product Code | FAS — Electrode, Electrosurgical, Active, Urological |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.4300 |