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ERGOSONIX ULTRASOUND SCANNER, MODULO ULTRASOUND SCANNER

K042326 Class II Traditional
Decision Date
2004-09-16
Sponsor / Applicant
Ultrasonix Medical Corporation

Technical Specification

510(k) Submission ID K042326
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2004-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ERGOSONIX ULTRASOUND SCANNER, MODULO ULTRASOUND SCANNER received FDA 510(k) clearance under submission number K042326, sponsored by Ultrasonix Medical 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 2004-09-16.

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.