Clearance Summary
CONTACT LENSES METRO-G 3X (HIOXIFILCON B) received FDA 510(k) clearance under submission number K964902, sponsored by Metro Optics of Austin, 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 1997-03-11.
- Submission: K964902
- Applicant / Sponsor: Metro Optics of Austin, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.5925
- Decision date: 1997-03-11
Classification & Regulation
This clearance is catalogued under FDA product code LPL and 21 CFR 886.5925, within the Ophthalmic review panel as a Class II device.