Clearance Summary
Oculeve Intranasal Tear Neurostimulator Device received FDA 510(k) clearance under submission number DEN160030, sponsored by Oculeve, 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 2017-04-24.
- Submission: DEN160030
- Applicant / Sponsor: Oculeve, Inc.
- Clearance pathway: Direct
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.5300
- Decision date: 2017-04-24
Classification & Regulation
This clearance is catalogued under FDA product code PQJ and 21 CFR 886.5300, within the Ophthalmic review panel as a Class II device.