meddevicedb.com FDA Device Reference

TRAVEL PAL (MM-111B) /MEGA MOTION

K060697 Class II Special
Decision Date
2006-04-11
Sponsor / Applicant
Mega Motion, Inc.

Technical Specification

510(k) Submission ID K060697
Product Code INI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3800
Decision Date 2006-04-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRAVEL PAL (MM-111B) /MEGA MOTION received FDA 510(k) clearance under submission number K060697, sponsored by Mega Motion, Inc.. 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 2006-04-11.

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.