syngo.CT Applications
K-Number: K232136 · 2024-01-04
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2024-01-04
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
syngo.CT Applications is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2024-01-04 under approval number K232136. 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 Applications?
syngo.CT Applications is a medical device that received FDA 510(k) clearance on 2024-01-04. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K232136.
When was syngo.CT Applications approved by the FDA?
syngo.CT Applications received FDA 510(k) clearance on 2024-01-04, under approval number K232136.
What company makes syngo.CT Applications?
syngo.CT Applications is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for syngo.CT Applications?
The FDA product code for syngo.CT Applications 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.