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IKON 40 Manual Wheelchair

K190550 Class I Traditional
Decision Date
2019-07-01
Sponsor / Applicant
Broda Seating (Broda Lp)

Technical Specification

510(k) Submission ID K190550
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2019-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IKON 40 Manual Wheelchair received FDA 510(k) clearance under submission number K190550, sponsored by Broda Seating (Broda Lp). 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 2019-07-01.

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.