ALOKA SSD-1000 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS ASU-1003, UST-9121, UST-9124— 510(k) K020668

Name: FDA 510(k) clearance K020668
Creator: U.S. Food and Drug Administration
Published: 2002-07-10

Substantially Equivalent

Aloka Co., Ltd.

FDA 510(k) clearance K020668 for ALOKA SSD-1000 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS ASU-1003, UST-9121, UST-9124, Substantially Equivalent on 2002-07-10. Applicant: Aloka Co., Ltd.. Device class: 2.

Clearance details

Applicant: Aloka Co., Ltd.
Product code: Code IYO
Device class: Class 2
Regulation: 21 CFR 892.1560
Advisory panel: Radiology
Date received: 2002-03-01
Decision date: 2002-07-10
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Wallingford, CT, US

Download summary PDF View on FDA.gov ↗

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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.