LungQ Software— 510(k) K173821

Substantially Equivalent

Thirona Corporation

FDA 510(k) clearance K173821 for LungQ Software, Substantially Equivalent on 2018-06-05. Applicant: Thirona Corporation.

Clearance details

Applicant: Thirona Corporation
Product code: Code JAK
Advisory panel: Radiology
Date received: 2017-12-18
Decision date: 2018-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nijmegen, NL

Download summary PDF View on FDA.gov ↗

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.