Clearance Summary
Alcon 27GA Chandelier (8065000252); Alcon 27+ DS Wide Angle Endoilluminator (8065000253); Alcon 27+ DS Endoilluminator (8065000256); received FDA 510(k) clearance under submission number K242184, sponsored by Alcon Laboratories, 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 2024-12-04.
- Submission: K242184
- Applicant / Sponsor: Alcon Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2024-12-04
Classification & Regulation
This clearance is catalogued under FDA product code MPA and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.