PQJ
- Product code
- PQJ
- Device name
- Intranasal Electrostimulation Device
- Device class
- Class 2
- 21 CFR
- 21 CFR 886.5300
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K)
- 510(k) clearances (all years, FDA)
- 1 (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 in adult patients.
Official FDA classification page: PQJ
Classification and pathway per current FDA publications. Data from openFDA (CC0).