syngo.CT LVO Detection
K-Number: K243145 · 2025-04-10
Device Summary
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. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K243145.
When did syngo.CT LVO Detection receive FDA 510(k) clearance?
syngo.CT LVO Detection received FDA 510(k) clearance on 2025-04-10, under 510(k) number K243145.
Who is the listed applicant for syngo.CT LVO Detection?
The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for syngo.CT LVO Detection?
The FDA product code for syngo.CT LVO Detection is QAS.
Other records listing Siemens Medical Solutions USA, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: QAS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.