meddevicedb.com FDA Device Reference

Electric Wheelchair, Model: 9000N

K221799 Class II Traditional
Decision Date
2022-09-16
Sponsor / Applicant
Silver Fox Corporation Limited

Technical Specification

510(k) Submission ID K221799
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2022-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electric Wheelchair, Model: 9000N received FDA 510(k) clearance under submission number K221799, sponsored by Silver Fox Corporation Limited. 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 2022-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code ITI and 21 CFR 890.3860, within the Physical Medicine review panel as a Class II device.