DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020, GI VERSION— 510(k) K920664

Substantially Equivalent

Diagnostic Ultrasound Corp.

FDA 510(k) clearance K920664 for DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020, GI VERSION, Substantially Equivalent on 1993-12-23. Applicant: Diagnostic Ultrasound Corp..

Clearance details

Applicant: Diagnostic Ultrasound Corp.
Product code: Code FFX
Advisory panel: Gastroenterology, Urology
Date received: 1992-02-13
Decision date: 1993-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kirkland, WA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FFX

product code FFX

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.