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DIAGNOSTIC ULTRASOUND UFS 1005

K902408 Class II Traditional
Decision Date
1990-08-10
Sponsor / Applicant
Diagnostic Ultrasound Corp.

Technical Specification

510(k) Submission ID K902408
Product Code EXY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1800
Decision Date 1990-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIAGNOSTIC ULTRASOUND UFS 1005 received FDA 510(k) clearance under submission number K902408, sponsored by Diagnostic Ultrasound Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1990-08-10.

Classification & Regulation

This clearance is catalogued under FDA product code EXY and 21 CFR 876.1800, within the Gastroenterology, Urology review panel as a Class II device.