Clearance Summary
PROTECTISCOPE CS COLONOSCOPE, NON-INTRAPULL received FDA 510(k) clearance under submission number K081004, sponsored by Stryker GI. 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 2008-05-02.
- Submission: K081004
- Applicant / Sponsor: Stryker GI
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2008-05-02
Classification & Regulation
This clearance is catalogued under FDA product code FDF and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.