Clearance Summary
GI Genius Module 100 (GGM100.US); GI Genius Module 200 (GGM200.US); ColonPRO 4.0 (CPRO40.US); GI Genius Module 300 (GGM300-US); ColonPRO 4.0 (CPRO40S-US) received FDA 510(k) clearance under submission number K241887, sponsored by Cosmo Artificial Intelligence - Ai, Ltd.. 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 2024-07-25.
- Submission: K241887
- Applicant / Sponsor: Cosmo Artificial Intelligence - Ai, Ltd.
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1520
- Decision date: 2024-07-25
Classification & Regulation
This clearance is catalogued under FDA product code QNP and 21 CFR 876.1520, within the Gastroenterology, Urology review panel as a Class II device.