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CTS-7700 DIGITAL ULTRASOUND IMAGING SYSTEM

K070982 Class II Traditional
Decision Date
2007-05-02
Sponsor / Applicant
Shantou Institute of Ultrasonic Instuments

Technical Specification

510(k) Submission ID K070982
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 2007-05-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CTS-7700 DIGITAL ULTRASOUND IMAGING SYSTEM received FDA 510(k) clearance under submission number K070982, sponsored by Shantou Institute of Ultrasonic Instuments. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2007-05-02.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.