meddevicedb.com FDA Device Reference

EASYTRAVEL

K012592 Class II Traditional
Decision Date
2001-10-03
Sponsor / Applicant
Tzora Active Systems , Ltd.

Technical Specification

510(k) Submission ID K012592
Product Code INI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3800
Decision Date 2001-10-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASYTRAVEL received FDA 510(k) clearance under submission number K012592, sponsored by Tzora Active Systems , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2001-10-03.

Classification & Regulation

This clearance is catalogued under FDA product code INI and 21 CFR 890.3800, within the Physical Medicine review panel as a Class II device.