K931764 is an FDA 510(k) clearance for the HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES. This device is classified as a Hysteroscope (and Accessories) (Class II - Special Controls, product code HIH).
Submitted by Olympus Corp. (Lake Success, US). The FDA issued a Cleared decision on June 8, 1994, 426 days after receiving the submission on April 8, 1993.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.1690.
| 510(k) Number | K931764 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 08, 1993 |
| Decision Date | June 08, 1994 |
| Days to Decision | 426 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | HIH — Hysteroscope (and Accessories) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.1690 |