Clearance Summary
2-Way 100% Silicone ClearTract Catheter received FDA 510(k) clearance under submission number K221625, sponsored by Silq Technologies Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2022-07-01.
- Submission: K221625
- Applicant / Sponsor: Silq Technologies Corporation
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5130
- Decision date: 2022-07-01
Classification & Regulation
This clearance is catalogued under FDA product code EZL and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.