meddevicedb.com FDA Device Reference

BREEZE

K051028 Class II Traditional
Decision Date
2006-01-27
Sponsor / Applicant
Afikim Electric Vehicles

Technical Specification

510(k) Submission ID K051028
Product Code INI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3800
Decision Date 2006-01-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BREEZE received FDA 510(k) clearance under submission number K051028, sponsored by Afikim Electric Vehicles. 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 2006-01-27.

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.