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INTELECT LEGEND ULTRASOUND

K973024 Class II Traditional
Decision Date
1997-11-10
Sponsor / Applicant
Chattanooga Group, Inc.

Technical Specification

510(k) Submission ID K973024
Product Code IMI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5300
Decision Date 1997-11-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTELECT LEGEND ULTRASOUND received FDA 510(k) clearance under submission number K973024, sponsored by Chattanooga Group, 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 1997-11-10.

Classification & Regulation

This clearance is catalogued under FDA product code IMI and 21 CFR 890.5300, within the Physical Medicine review panel as a Class II device.