K172217 is an FDA 510(k) clearance for the Flexor Ureteral Access Sheath and Flexor Parallel Rapid Release Ureteral Access Sheath. This device is classified as a Endoscopic Access Overtube, Gastroenterology-urology (Class II - Special Controls, product code FED).
Submitted by Cook Incorporated (Bloomington, US). The FDA issued a Cleared decision on December 13, 2017, 142 days after receiving the submission on July 24, 2017.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1500. To Facilitate Passage And Aid Advancement Of Endoscopes Into The Body, Especially In Cases Of Repeated Intubation..
| 510(k) Number | K172217 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 24, 2017 |
| Decision Date | December 13, 2017 |
| Days to Decision | 142 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FED — Endoscopic Access Overtube, Gastroenterology-urology |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.1500 |
| Definition | To Facilitate Passage And Aid Advancement Of Endoscopes Into The Body, Especially In Cases Of Repeated Intubation. |