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HEARTWAY LIGHTWEIGHT POWER MOBILITY SCOOTER, S34

K101142 Class II Traditional
Decision Date
2010-05-26
Sponsor / Applicant
Heartway Medical Products Co., Ltd.

Technical Specification

510(k) Submission ID K101142
Product Code INI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3800
Decision Date 2010-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEARTWAY LIGHTWEIGHT POWER MOBILITY SCOOTER, S34 received FDA 510(k) clearance under submission number K101142, 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 2010-05-26.

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.