meddevicedb.com FDA Device Reference

SOFTIQUE, MODEL GI 11001

K013707 Class II Traditional
Decision Date
2002-02-01
Sponsor / Applicant
Global TV Concepts, Ltd.

Technical Specification

510(k) Submission ID K013707
Product Code IMC
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5110
Decision Date 2002-02-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOFTIQUE, MODEL GI 11001 received FDA 510(k) clearance under submission number K013707, sponsored by Global TV Concepts, Ltd.. 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 2002-02-01.

Classification & Regulation

This clearance is catalogued under FDA product code IMC and 21 CFR 890.5110, within the Physical Medicine review panel as a Class II device.