meddevicedb.com FDA Device Reference

MAXHEALTH WHEELCHAIR, MODEL HE-8631, HE-8621, HE-8651

K001252 Class I Traditional
Decision Date
2000-06-12
Sponsor / Applicant
Maxhealth Corp.

Technical Specification

510(k) Submission ID K001252
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2000-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAXHEALTH WHEELCHAIR, MODEL HE-8631, HE-8621, HE-8651 received FDA 510(k) clearance under submission number K001252, sponsored by Maxhealth Corp.. 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 2000-06-12.

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.