K972856 is an FDA 510(k) clearance for the ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLS. This device is classified as a Coagulator-cutter, Endoscopic, Unipolar (and Accessories) (Class II - Special Controls, product code KNF).
Submitted by Rocket Medical Plc (Washington, GB). The FDA issued a Cleared decision on February 11, 1998, 194 days after receiving the submission on August 1, 1997.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.4160.
| 510(k) Number | K972856 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 01, 1997 |
| Decision Date | February 11, 1998 |
| Days to Decision | 194 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | KNF — Coagulator-cutter, Endoscopic, Unipolar (and Accessories) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.4160 |