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BRIX WHEELCHAIR

K050941 Class I Traditional
Decision Date
2005-05-05
Sponsor / Applicant
Meyra, Inc.

Technical Specification

510(k) Submission ID K050941
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2005-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BRIX WHEELCHAIR received FDA 510(k) clearance under submission number K050941, sponsored by Meyra, 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 2005-05-05.

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.