syngo.CT LVO Detection
K-Number: K243145 · 2025-04-10
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2025-04-10
Product CodeQAS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
syngo.CT LVO Detection is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2025-04-10 under approval number K243145. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the syngo.CT LVO Detection?
syngo.CT LVO Detection is a medical device that received FDA 510(k) clearance on 2025-04-10. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K243145.
When was syngo.CT LVO Detection approved by the FDA?
syngo.CT LVO Detection received FDA 510(k) clearance on 2025-04-10, under approval number K243145.
What company makes syngo.CT LVO Detection?
syngo.CT LVO Detection is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for syngo.CT LVO Detection?
The FDA product code for syngo.CT LVO Detection is QAS.
Other Devices by Siemens Medical Solutions USA, Inc.
Related Devices (Code: QAS)
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.