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SONOACE X8 DIAGNOSTIC ULTRASOUND SYSTEM

K093714 Class II Traditional
Decision Date
2009-12-10
Sponsor / Applicant
Medison Co., Ltd.

Technical Specification

510(k) Submission ID K093714
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2009-12-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONOACE X8 DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance under submission number K093714, sponsored by Medison Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2009-12-10.

Classification & Regulation

This clearance is catalogued under FDA product code ITX and 21 CFR 892.1570, within the Radiology review panel as a Class II device.