meddevicedb.com FDA Device Reference

VIEWMATE SYSTEM

K071028 Class I Special
Decision Date
2007-05-01
Sponsor / Applicant
Ep Medsystems

Technical Specification

510(k) Submission ID K071028
Product Code ITN
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3675
Decision Date 2007-05-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VIEWMATE SYSTEM received FDA 510(k) clearance under submission number K071028, sponsored by Ep Medsystems. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2007-05-01.

Classification & Regulation

This clearance is catalogued under FDA product code ITN and 21 CFR 890.3675, within the Physical Medicine review panel as a Class I device.