meddevicedb.com FDA Device Reference

TRAVEL EASE

K933406 Class I Traditional
Decision Date
1993-09-30
Sponsor / Applicant
Merits Health Products., Inc.

Technical Specification

510(k) Submission ID K933406
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 1993-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRAVEL EASE received FDA 510(k) clearance under submission number K933406, sponsored by Merits Health Products., Inc.. 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 1993-09-30.

Classification & Regulation

This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.