Clearance Summary
ICATH, STERILESURE received FDA 510(k) clearance under submission number K071496, sponsored by Colorado Catheter Company, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2007-08-15.
- Submission: K071496
- Applicant / Sponsor: Colorado Catheter Company, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5130
- Decision date: 2007-08-15
Classification & Regulation
This clearance is catalogued under FDA product code NWO and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.