meddevicedb.com FDA Device Reference

MEDX MACHINE

K911666 Class II Traditional
Decision Date
1991-07-03
Sponsor / Applicant
Medx Corp.

Technical Specification

510(k) Submission ID K911666
Product Code IKK
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.1925
Decision Date 1991-07-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDX MACHINE received FDA 510(k) clearance under submission number K911666, sponsored by Medx Corp.. 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 1991-07-03.

Classification & Regulation

This clearance is catalogued under FDA product code IKK and 21 CFR 890.1925, within the Physical Medicine review panel as a Class II device.