meddevicedb.com FDA Device Reference

ADD'L TRANSDUCER FOR USE W/EUB-165 ULTRASOUND

K901658 Class II Traditional
Decision Date
1990-09-04
Sponsor / Applicant
Hitachi Medical Corp. of America

Technical Specification

510(k) Submission ID K901658
Product Code DXK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2330
Decision Date 1990-09-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADD'L TRANSDUCER FOR USE W/EUB-165 ULTRASOUND received FDA 510(k) clearance under submission number K901658, sponsored by Hitachi Medical Corp. of America. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1990-09-04.

Classification & Regulation

This clearance is catalogued under FDA product code DXK and 21 CFR 870.2330, within the Cardiovascular review panel as a Class II device.