meddevicedb.com FDA Device Reference

UST-2266U-5 CW DOPPLER TRANSDUCER

K905369 Class II Traditional
Decision Date
1991-02-11
Sponsor / Applicant
Ge Medical Systems Information Technologies

Technical Specification

510(k) Submission ID K905369
Product Code JOP
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2880
Decision Date 1991-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UST-2266U-5 CW DOPPLER TRANSDUCER received FDA 510(k) clearance under submission number K905369, sponsored by Ge Medical Systems Information Technologies. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-02-11.

Classification & Regulation

This clearance is catalogued under FDA product code JOP and 21 CFR 870.2880, within the Cardiovascular review panel as a Class II device.