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Devices · Siemens Healthcare GmbH

syngo.CT Lung CAD

510(k)K203258RadiologyOEB

Siemens Healthcare GmbH is listed for syngo.CT Lung CAD (K203258). The FDA list gives March 31, 2021 as the date of the final decision. The lead panel is Radiology, and the database link on the FDA list is the 510(k) pathway. openFDA describes product code OEB as “Lung Computed Tomography System, Computer-Aided Detection”: To assist radiologists in the review of multi-slice computed tomography (msct) exams of the chest and highlight potential nodules that the radiologist should review. A computer aided diagnosis, lung computed tomography system is a class 3 device under product code NRR. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K203258

Official FDA database record

Date of final decision
March 31, 2021
Company on the FDA list
Siemens Healthcare GmbH
Lead panel
Radiology
Primary product code
OEB
openFDA device name for the code
Lung Computed Tomography System, Computer-Aided Detection
Device class
2
Regulation number
892.2050
openFDA decision description
Substantially Equivalent
openFDA decision code
SESE
Statement or summary label
Summary

Product-code text from openFDA

To assist radiologists in the review of multi-slice computed tomography (msct) exams of the chest and highlight potential nodules that the radiologist should review. A computer aided diagnosis, lung computed tomography system is a class 3 device under product code NRR.

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