meddevicedb.com FDA Device Reference

EUB-6000 ULTRASOUND DIAGNOSTIC SCANNER

K994026 Class II Traditional
Decision Date
2000-03-29
Sponsor / Applicant
Hitachi Medical Corp. of America

Technical Specification

510(k) Submission ID K994026
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2000-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EUB-6000 ULTRASOUND DIAGNOSTIC SCANNER received FDA 510(k) clearance under submission number K994026, sponsored by Hitachi Medical Corp. of America. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-03-29.

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.