LOGIQ A200 DIAGNOSTIC ULTRASOUND SYSTEM— 510(k) K960700

Substantially Equivalent

GE Medical Systems

FDA 510(k) clearance K960700 for LOGIQ A200 DIAGNOSTIC ULTRASOUND SYSTEM, Substantially Equivalent on 1996-08-28. Applicant: GE Medical Systems.

Clearance details

Applicant: GE Medical Systems
Product code: Code IYO
Advisory panel: Radiology
Date received: 1996-02-20
Decision date: 1996-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

Download summary PDF View on FDA.gov ↗

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.