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MULTI FRAME WHEELCHAIR

K100084 Class I Traditional
Decision Date
2010-04-12
Sponsor / Applicant
R82 A/S

Technical Specification

510(k) Submission ID K100084
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2010-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTI FRAME WHEELCHAIR received FDA 510(k) clearance under submission number K100084, sponsored by R82 A/S. 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 2010-04-12.

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.