syngo.CT Dual Energy
K-Number: K232155 · 2023-11-30
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2023-11-30
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
syngo.CT Dual Energy is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2023-11-30 under approval number K232155. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the syngo.CT Dual Energy?
syngo.CT Dual Energy is a medical device that received FDA 510(k) clearance on 2023-11-30. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K232155.
When was syngo.CT Dual Energy approved by the FDA?
syngo.CT Dual Energy received FDA 510(k) clearance on 2023-11-30, under approval number K232155.
What company makes syngo.CT Dual Energy?
syngo.CT Dual Energy is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for syngo.CT Dual Energy?
The FDA product code for syngo.CT Dual Energy is JAK.
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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.