Classic Cotton Cannulatome®, CannulaTome II® Double Lumen Sphincterotome, Cotton CannulaTome II® PC, UTS® Ultra Taper Sphincterotome, Tri-Tome pc® Triple Lumen Sphincterotome, Howell D.A.S.H.® Sphincterotome with DomeTip®, Billroth II Sphincterotome, Soehendra® BII Sphincterotome, Models ACU-1 and ACU-1-VL active cords
K172665 is the FDA 510(k) clearance record for Classic Cotton Cannulatome®, CannulaTome II® Double Lumen Sphincterotome, Cotton CannulaTome II® PC, UTS® Ultra Taper Sphincterotome, Tri-Tome pc® Triple Lumen Sphincterotome, Howell D.A.S.H.® Sphincterotome with DomeTip®, Billroth II Sphincterotome, Soehendra® BII Sphincterotome, Models ACU-1 and ACU-1-VL active cords, a class II device, cleared for Wilson-Cook Medical Inc./Cook Endoscopy on under FDA product code KNS (Unit, Electrosurgical, Endoscopic (With Or Without Accessories)). FDA records list 7 510(k) clearances for Wilson-Cook Medical Inc./Cook Endoscopy, from to . As of , FDA records show no recalls naming K172665.
Clearance record
- Decision date
- Received
- (261 days to decision)
- Product code
- KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
- Regulation
- 21 CFR 876.4300
- Device class
- Class II
- Review panel
- Gastroenterology, Urology
- Applicant
- Wilson-Cook Medical Inc./Cook Endoscopy 4900 Bethania Station Rd., Winston-Salem NC
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code KNS
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 2 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 1 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| October 2026 | 0 |
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