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EZZIE SYSTEM

K851740 Class II Traditional
Decision Date
1985-07-15
Sponsor / Applicant
Independent Living, Inc.

Technical Specification

510(k) Submission ID K851740
Product Code IQA
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3725
Decision Date 1985-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EZZIE SYSTEM received FDA 510(k) clearance under submission number K851740, sponsored by Independent Living, Inc.. 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 1985-07-15.

Classification & Regulation

This clearance is catalogued under FDA product code IQA and 21 CFR 890.3725, within the Physical Medicine review panel as a Class II device.