Clearance Summary
FloNavi Endoscopic Fluorescence Imaging System received FDA 510(k) clearance under submission number K221861, sponsored by Guangdong Optomedic Technologies, 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 2023-02-18.
- Submission: K221861
- Applicant / Sponsor: Guangdong Optomedic Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2023-02-18
Classification & Regulation
This clearance is catalogued under FDA product code GCJ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.