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NON-CONTACT TEAR FILM THERMOGRAGH

K111771 Class II Traditional
Decision Date
2011-11-30
Sponsor / Applicant
United Integrated Services Co., Ltd.

Technical Specification

510(k) Submission ID K111771
Product Code HKI
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1120
Decision Date 2011-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NON-CONTACT TEAR FILM THERMOGRAGH received FDA 510(k) clearance under submission number K111771, sponsored by United Integrated Services Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2011-11-30.

Classification & Regulation

This clearance is catalogued under FDA product code HKI and 21 CFR 886.1120, within the Ophthalmic review panel as a Class II device.