DIAGNOSTIC ULTRASOUND/URO-GYN UDS 2000 SERIES— 510(k) K911091

Name: FDA 510(k) clearance K911091
Creator: U.S. Food and Drug Administration
Published: 1991-06-10

Substantially Equivalent

Diagnostic Ultrasound Corp.

FDA 510(k) clearance K911091 for DIAGNOSTIC ULTRASOUND/URO-GYN UDS 2000 SERIES, Substantially Equivalent on 1991-06-10. Applicant: Diagnostic Ultrasound Corp.. Device class: 2.

Clearance details

Applicant: Diagnostic Ultrasound Corp.
Product code: Code FAP
Device class: Class 2
Regulation: 21 CFR 876.1620
Advisory panel: Gastroenterology, Urology
Date received: 1991-03-12
Decision date: 1991-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kirkland, WA, US

Download summary PDF View on FDA.gov ↗

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