meddevicedb.com FDA Device Reference

Ultravision Visual Field Clearing System

K200035 Class II Traditional
Decision Date
2020-05-04
Sponsor / Applicant
Alesi Surgical, Ltd.

Technical Specification

510(k) Submission ID K200035
Product Code PQM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5050
Decision Date 2020-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ultravision Visual Field Clearing System received FDA 510(k) clearance under submission number K200035, sponsored by Alesi Surgical, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2020-05-04.

Classification & Regulation

This clearance is catalogued under FDA product code PQM and 21 CFR 878.5050, within the General, Plastic Surgery review panel as a Class II device.