GE LOGIQ 500 DIAGNOSTIC ULTRASOUND SYSTEM— 510(k) K970901

Name: FDA 510(k) clearance K970901
Creator: U.S. Food and Drug Administration
Published: 1997-12-22

Substantially Equivalent

GE Medical Systems

FDA 510(k) clearance K970901 for GE LOGIQ 500 DIAGNOSTIC ULTRASOUND SYSTEM, Substantially Equivalent on 1997-12-22. Applicant: GE Medical Systems. Device class: 2.

Clearance details

Applicant: GE Medical Systems
Product code: Code IYO
Device class: Class 2
Regulation: 21 CFR 892.1560
Advisory panel: Radiology
Date received: 1997-03-11
Decision date: 1997-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, 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.