meddevicedb.com FDA Device Reference

CLEAR-IT ANTI-FOG, MODEL PS003

K022826 Class II Traditional
Decision Date
2002-10-09
Sponsor / Applicant
Preservation Solutions, Inc.

Technical Specification

510(k) Submission ID K022826
Product Code OCT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2002-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEAR-IT ANTI-FOG, MODEL PS003 received FDA 510(k) clearance under submission number K022826, sponsored by Preservation Solutions, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2002-10-09.

Classification & Regulation

This clearance is catalogued under FDA product code OCT and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.