HISPEED LX//I, HISPEED FX/I, AND HISPEED DX/I FAMILY OF SYSTEMS— 510(k) K980169

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K980169 for HISPEED LX//I, HISPEED FX/I, AND HISPEED DX/I FAMILY OF SYSTEMS, Substantially Equivalent on 1998-04-13. Applicant: General Electric Co..

Clearance details

Applicant: General Electric Co.
Product code: Code JAK
Advisory panel: Radiology
Date received: 1998-01-16
Decision date: 1998-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

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Adverse events under product code JAK

product code JAK

Death: 27
Injury: 571
Malfunction: 779
Total: 1,377

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.