CT-C3000 SPIRAL CT SCANNER SYSTEM— 510(k) K020913

Substantially Equivalent

Neusoft Digital Medical Systems Co., Ltd.

FDA 510(k) clearance K020913 for CT-C3000 SPIRAL CT SCANNER SYSTEM, Substantially Equivalent on 2002-04-03. Applicant: Neusoft Digital Medical Systems Co., Ltd..

Clearance details

Applicant: Neusoft Digital Medical Systems Co., Ltd.
Product code: Code JAK
Advisory panel: Radiology
Date received: 2002-03-21
Decision date: 2002-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenyang, Liaoning, CN

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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.