meddevicedb.com FDA Device Reference

TearCare System

K213045 Class II Traditional
Decision Date
2021-12-21
Sponsor / Applicant
Sight Sciences, Inc.

Technical Specification

510(k) Submission ID K213045
Product Code ORZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5200
Decision Date 2021-12-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TearCare System received FDA 510(k) clearance under submission number K213045, sponsored by Sight Sciences, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2021-12-21.

Classification & Regulation

This clearance is catalogued under FDA product code ORZ and 21 CFR 886.5200, within the Ophthalmic review panel as a Class II device.