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EUB-5500 DIAGNOSTIC ULTRASOUND SCANNER

K032503 Class II Special
Decision Date
2003-08-22
Sponsor / Applicant
Hitachi Medical Systems America, Inc.

Technical Specification

510(k) Submission ID K032503
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2003-08-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EUB-5500 DIAGNOSTIC ULTRASOUND SCANNER received FDA 510(k) clearance under submission number K032503, sponsored by Hitachi Medical Systems America, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2003-08-22.

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.