SSI-600/SSI-800 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM— 510(k) K041455

Name: FDA 510(k) clearance K041455
Creator: U.S. Food and Drug Administration
Published: 2004-06-10

Substantially Equivalent

Sonoscape Company Limited

FDA 510(k) clearance K041455 for SSI-600/SSI-800 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM, Substantially Equivalent on 2004-06-10. Applicant: Sonoscape Company Limited. Device class: 2.

Clearance details

Applicant: Sonoscape Company Limited
Product code: Code IYO
Device class: Class 2
Regulation: 21 CFR 892.1560
Advisory panel: Radiology
Date received: 2004-06-01
Decision date: 2004-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dublin, CA, 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.