K930733 is an FDA 510(k) clearance for the URETERAL STENT. This device is classified as a Stent, Ureteral (Class II - Special Controls, product code FAD).
Submitted by Surgitek (Racine, US). The FDA issued a Cleared decision on July 23, 1993, 162 days after receiving the submission on February 11, 1993.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.4620.
| 510(k) Number | K930733 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 11, 1993 |
| Decision Date | July 23, 1993 |
| Days to Decision | 162 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Statement |
| Product Code | FAD — Stent, Ureteral |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.4620 |