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VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM

K031077 Class II Traditional
Decision Date
2003-12-11
Sponsor / Applicant
Chattanooga Group

Technical Specification

510(k) Submission ID K031077
Product Code IMG
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5860
Decision Date 2003-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM received FDA 510(k) clearance under submission number K031077, sponsored by Chattanooga Group. 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 2003-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code IMG and 21 CFR 890.5860, within the Physical Medicine review panel as a Class II device.