Clearance Summary
VX130 Ophthalmic Diagnostic Device received FDA 510(k) clearance under submission number K162067, sponsored by Luneau Sas. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2017-04-24.
- Submission: K162067
- Applicant / Sponsor: Luneau Sas
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1930
- Decision date: 2017-04-24
Classification & Regulation
This clearance is catalogued under FDA product code HKX and 21 CFR 886.1930, within the Ophthalmic review panel as a Class II device.