Allia Moveo
K-Number: K251199 · 2025-12-09
ApplicantGE Medical Systems SCS
Decision Date2025-12-09
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Allia Moveo is a medical device manufactured by GE Medical Systems SCS. It received FDA 510(k) clearance on 2025-12-09 under approval number K251199. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Allia Moveo?
Allia Moveo is a medical device that received FDA 510(k) clearance on 2025-12-09. It is manufactured by GE Medical Systems SCS. The 510(k) number is K251199.
When was Allia Moveo approved by the FDA?
Allia Moveo received FDA 510(k) clearance on 2025-12-09, under approval number K251199.
What company makes Allia Moveo?
Allia Moveo is manufactured by GE Medical Systems SCS.
What is the FDA product code for Allia Moveo?
The FDA product code for Allia Moveo is OWB.
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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.