Clearance Summary
Ahmed® Glaucoma Valve Model FP8 received FDA 510(k) clearance under submission number K231051, sponsored by New World Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2023-05-12.
- Submission: K231051
- Applicant / Sponsor: New World Medical, Inc.
- Clearance pathway: Special
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.3920
- Decision date: 2023-05-12
Classification & Regulation
This clearance is catalogued under FDA product code KYF and 21 CFR 886.3920, within the Ophthalmic review panel as a Class II device.