# Intranasal Electrostimulation Device For Dry Eye Symptoms
> **Product code: QBR** · Class II — Moderate Risk (510(k) clearance required) · Ophthalmic · 21 CFR 886.5310
## Classification
- **FDA Product Code:** QBR
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 886.5310
- **Review panel:** OP
- **Medical specialty:** Ophthalmic
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Definition

This device type is intended to temporarily increase tear production using neurostimulation to improve dry eye symptoms. For prescription use only.

## Market data
- **Cleared 510(k) submissions:** 2
- **Registered establishments:** 0
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=QBR)
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