Clearance Summary
FUJIFILM Endoscope Models EC-600HL and EC-600LS received FDA 510(k) clearance under submission number K180405, sponsored by Fujifilm Corporation. 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 2018-03-15.
- Submission: K180405
- Applicant / Sponsor: Fujifilm Corporation
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2018-03-15
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.