Clearance Summary
FLEXIBLE LIQUID LIGHT GUIDE received FDA 510(k) clearance under submission number K834487, sponsored by Endo Lase, 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 1984-02-21.
- Submission: K834487
- Applicant / Sponsor: Endo Lase, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1984-02-21
Classification & Regulation
This clearance is catalogued under FDA product code FFS and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.