Product code QBR
- Device name
- Intranasal Electrostimulation Device For Dry Eye Symptoms
- Medical specialty
- Ophthalmic
- Device class
- 2
- Regulation number
- 886.5310
- Review panel
- OP
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Ineligible
- Definition
- This device type is intended to temporarily increase tear production using neurostimulation to improve dry eye symptoms. For prescription use only.
- Source
- FDA openFDA device classification dataset