meddevicedb.com FDA Device Reference

X2000 TRADITIONAL WHEELCHAIR

K951351 Class I Traditional
Decision Date
1995-04-26
Sponsor / Applicant
Homecrest Industries

Technical Specification

510(k) Submission ID K951351
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 1995-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X2000 TRADITIONAL WHEELCHAIR received FDA 510(k) clearance under submission number K951351, sponsored by Homecrest Industries. 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 1995-04-26.

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.