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ELECTRIC WHEELCHAIR, MODEL RUMBA S (HP4)

K063203 Class II Abbreviated
Decision Date
2007-02-13
Sponsor / Applicant
Imc-Heart Way LLC

Technical Specification

510(k) Submission ID K063203
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2007-02-13
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRIC WHEELCHAIR, MODEL RUMBA S (HP4) received FDA 510(k) clearance under submission number K063203, sponsored by Imc-Heart Way LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2007-02-13.

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.