Clearance Summary
MAXReach Laser Probe received FDA 510(k) clearance under submission number K191846, sponsored by Vortex Surgical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2019-12-23.
- Submission: K191846
- Applicant / Sponsor: Vortex Surgical, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4690
- Decision date: 2019-12-23
Classification & Regulation
This clearance is catalogued under FDA product code HQB and 21 CFR 886.4690, within the Ophthalmic review panel as a Class II device.