syngo.CT Lung CAD (Version VD30)
K-Number: K231157 · 2023-07-19
ApplicantSiemens Healthcare GmbH
Decision Date2023-07-19
Product CodeOEB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
syngo.CT Lung CAD (Version VD30) is a medical device manufactured by Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2023-07-19 under approval number K231157. The device is classified under product code OEB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the syngo.CT Lung CAD (Version VD30)?
syngo.CT Lung CAD (Version VD30) is a medical device that received FDA 510(k) clearance on 2023-07-19. It is manufactured by Siemens Healthcare GmbH. The 510(k) number is K231157.
When was syngo.CT Lung CAD (Version VD30) approved by the FDA?
syngo.CT Lung CAD (Version VD30) received FDA 510(k) clearance on 2023-07-19, under approval number K231157.
What company makes syngo.CT Lung CAD (Version VD30)?
syngo.CT Lung CAD (Version VD30) is manufactured by Siemens Healthcare GmbH.
What is the FDA product code for syngo.CT Lung CAD (Version VD30)?
The FDA product code for syngo.CT Lung CAD (Version VD30) is OEB.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.