Clearance Summary
DUALENZ LOW VISION EYEWEAR received FDA 510(k) clearance under submission number K864594, sponsored by Global Eye Care, 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 1987-01-20.
- Submission: K864594
- Applicant / Sponsor: Global Eye Care, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5870
- Decision date: 1987-01-20
Classification & Regulation
This clearance is catalogued under FDA product code HKK and 21 CFR 886.5870, within the Ophthalmic review panel as a Class I device.