Methinks CTA Stroke
K-Number: K251590 · 2025-08-20
ApplicantMethinks Software, S.L
Decision Date2025-08-20
Product CodeQAS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Methinks CTA Stroke is a medical device manufactured by Methinks Software, S.L. It received FDA 510(k) clearance on 2025-08-20 under approval number K251590. 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 Methinks CTA Stroke?
Methinks CTA Stroke is a medical device that received FDA 510(k) clearance on 2025-08-20. It is manufactured by Methinks Software, S.L. The 510(k) number is K251590.
When was Methinks CTA Stroke approved by the FDA?
Methinks CTA Stroke received FDA 510(k) clearance on 2025-08-20, under approval number K251590.
What company makes Methinks CTA Stroke?
Methinks CTA Stroke is manufactured by Methinks Software, S.L.
What is the FDA product code for Methinks CTA Stroke?
The FDA product code for Methinks CTA Stroke is QAS.
Other Devices by Methinks Software, S.L
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.