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Intranasal Electrostimulation Device For Dry Eye Symptoms

FDA product code QBR · 1 cleared devices

Class 2 Ophthalmic
Regulation
21 CFR 886.5310
Review panel
OP
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
2020-08-31 – 2020-08-31

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

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