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iTEAR100 Neurostimulator

K213623 Class II Traditional
Decision Date
2022-03-16
Sponsor / Applicant
Olympic Ophthalmics

Technical Specification

510(k) Submission ID K213623
Product Code QKV
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5305
Decision Date 2022-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

iTEAR100 Neurostimulator received FDA 510(k) clearance under submission number K213623, sponsored by Olympic Ophthalmics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2022-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code QKV and 21 CFR 886.5305, within the Ophthalmic review panel as a Class II device.