Oculeve Intranasal Tear Neurostimulator Device— 510(k) DEN160030
UnknownOculeve, Inc.
FDA 510(k) clearance DEN160030 for Oculeve Intranasal Tear Neurostimulator Device, Unknown on 2017-04-24. Applicant: Oculeve, Inc.. Device class: 2.
Clearance details
- Applicant
- Oculeve, Inc.
- Product code
- Code PQJ
- Device class
- Class 2
- Regulation
- 21 CFR 886.5300
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- South San Francisco, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.