meddevicedb.com FDA Device Reference

VS-100 ILLUMINATION AND IMAGING SYSTEM

K090800 Class II Traditional
Decision Date
2009-05-18
Sponsor / Applicant
Schoelly Imaging, Inc.

Technical Specification

510(k) Submission ID K090800
Product Code FET
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2009-05-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VS-100 ILLUMINATION AND IMAGING SYSTEM received FDA 510(k) clearance under submission number K090800, sponsored by Schoelly Imaging, 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 2009-05-18.

Classification & Regulation

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