DIAGNOSTIC ULTRASOUND/URO-GYN UDS 1002— 510(k) K902692

Name: FDA 510(k) clearance K902692
Creator: U.S. Food and Drug Administration
Published: 1990-09-13

Substantially Equivalent

Diagnostic Ultrasound Corp.

FDA 510(k) clearance K902692 for DIAGNOSTIC ULTRASOUND/URO-GYN UDS 1002, Substantially Equivalent on 1990-09-13. 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: 1990-06-19
Decision date: 1990-09-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kirkland, WA, US

Download summary PDF View on FDA.gov ↗

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