K061766 is an FDA 510(k) clearance for the EXPRESSWAY INTERMITTENT CATHETER. This device is classified as a Catheter, Straight (Class II - Special Controls, product code EZD).
Submitted by Percutaneous Systems, Incorporated (Mountain View, US). The FDA issued a Cleared decision on March 9, 2007, 260 days after receiving the submission on June 22, 2006.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5130.
| 510(k) Number | K061766 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 22, 2006 |
| Decision Date | March 09, 2007 |
| Days to Decision | 260 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | EZD — Catheter, Straight |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.5130 |