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DIGITAL COLOR DOPPLER ULTRASOUND IMAGING SYSTEM

K113613 Class II Traditional
Decision Date
2012-06-15
Sponsor / Applicant
Shantou Institute of Ultrasonic Instuments

Technical Specification

510(k) Submission ID K113613
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2012-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIGITAL COLOR DOPPLER ULTRASOUND IMAGING SYSTEM received FDA 510(k) clearance under submission number K113613, 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 2012-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.