QBR

Intranasal Electrostimulation Device For Dry Eye Symptoms

Product code

QBR

Device name

Intranasal Electrostimulation Device For Dry Eye Symptoms

Device class

Class 2

21 CFR

21 CFR 886.5310

Medical specialty

Ophthalmic

Marketing pathway

510(K)

510(k) clearances (all years, FDA)

2 (all years; only the last 3 years are listed here)

FDA classification definition

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

Definition text from the FDA device classification database (U.S. federal government work, public domain).