Clearance Summary
BRAINPORT V100 DEVICE received FDA 510(k) clearance under submission number DEN130039, sponsored by Wicab, Inc.. The device was reviewed via the Direct premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2015-06-18.
- Submission: DEN130039
- Applicant / Sponsor: Wicab, Inc.
- Clearance pathway: Direct
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.5905
- Decision date: 2015-06-18
Classification & Regulation
This clearance is catalogued under FDA product code PIC and 21 CFR 886.5905, within the Ophthalmic review panel as a Class II device.