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SOFIA AUTOMATED TOMOGRAPHIC ULTRASOUND (ATUS)

K080555 Class II Traditional
Decision Date
2008-06-03
Sponsor / Applicant
Ivu Imaging Corporation

Technical Specification

510(k) Submission ID K080555
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2008-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOFIA AUTOMATED TOMOGRAPHIC ULTRASOUND (ATUS) received FDA 510(k) clearance under submission number K080555, sponsored by Ivu Imaging Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2008-06-03.

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.