Clearance Summary
i3 ONE (203100-S);i3 TWO connect (203200-S);i3 TWO direct (203300-S) received FDA 510(k) clearance under submission number K222727, sponsored by I3 Membrane GmbH. 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 2023-06-02.
- Submission: K222727
- Applicant / Sponsor: I3 Membrane GmbH
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5665
- Decision date: 2023-06-02
Classification & Regulation
This clearance is catalogued under FDA product code NHV and 21 CFR 876.5665, within the Gastroenterology, Urology review panel as a Class II device.