DIAGNOSTIC ULTRASOUND UFS 1005— 510(k) K902408

Name: FDA 510(k) clearance K902408
Creator: U.S. Food and Drug Administration
Published: 1990-08-10

Substantially Equivalent

Diagnostic Ultrasound Corp.

FDA 510(k) clearance K902408 for DIAGNOSTIC ULTRASOUND UFS 1005, Substantially Equivalent on 1990-08-10. Applicant: Diagnostic Ultrasound Corp.. Device class: 2.

Clearance details

Applicant: Diagnostic Ultrasound Corp.
Product code: Code EXY
Device class: Class 2
Regulation: 21 CFR 876.1800
Advisory panel: Gastroenterology, Urology
Date received: 1990-05-31
Decision date: 1990-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kirkland, WA, US

Download summary PDF View on FDA.gov ↗

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