MODEL I0-3DUIMS 3D ULTRASOUND MANAGEMENT SYSTEM— 510(k) K011095

Substantially Equivalent

Iodp SA

FDA 510(k) clearance K011095 for MODEL I0-3DUIMS 3D ULTRASOUND MANAGEMENT SYSTEM, Substantially Equivalent on 2001-06-13. Applicant: Iodp SA.

Clearance details

Applicant: Iodp SA
Product code: Code IYO
Advisory panel: Radiology
Date received: 2001-04-10
Decision date: 2001-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, IL, 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.