DUS-3000/DUS-3000PLUS DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM— 510(k) K112022

Substantially Equivalent

Advanced Instrumentations, Inc.

FDA 510(k) clearance K112022 for DUS-3000/DUS-3000PLUS DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM, Substantially Equivalent on 2011-09-22. Applicant: Advanced Instrumentations, Inc..

Clearance details

Applicant: Advanced Instrumentations, Inc.
Product code: Code IYO
Advisory panel: Radiology
Date received: 2011-07-15
Decision date: 2011-09-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hialeah, FL, US

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Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

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.