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ECHO VIEW/SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM

K970508 Class II Traditional
Decision Date
1997-08-04
Sponsor / Applicant
Shimadzu Medical Systems

Technical Specification

510(k) Submission ID K970508
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 1997-08-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ECHO VIEW/SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance under submission number K970508, sponsored by Shimadzu Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1997-08-04.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.