K934835 is an FDA 510(k) clearance for the FLOVAL. This device is classified as a Resectoscope (Class II - Special Controls, product code FJL).
Submitted by Olympus Corp. (Lake Success, US). The FDA issued a Cleared decision on June 21, 1994, 256 days after receiving the submission on October 8, 1993.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K934835 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 08, 1993 |
| Decision Date | June 21, 1994 |
| Days to Decision | 256 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FJL — Resectoscope |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1500 |