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HEARTWAY POWER WHEELCHAIR

K132856 Class II Traditional
Decision Date
2014-07-15
Sponsor / Applicant
Heartway Medical Products Co., Ltd.

Technical Specification

510(k) Submission ID K132856
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2014-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEARTWAY POWER WHEELCHAIR received FDA 510(k) clearance under submission number K132856, sponsored by Heartway Medical Products Co., Ltd.. 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 2014-07-15.

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.