Clearance Summary
PATHWAY BALLOON EXPANDABLE URETERAL ACCESS SHEATH, MODEL BEUS received FDA 510(k) clearance under submission number K061009, sponsored by Onset Medical 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 2006-05-02.
- Submission: K061009
- Applicant / Sponsor: Onset Medical Corporation
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5470
- Decision date: 2006-05-02
Classification & Regulation
This clearance is catalogued under FDA product code EZN and 21 CFR 876.5470, within the Gastroenterology, Urology review panel as a Class II device.