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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems SCS. It received FDA 510(k) clearance on 2025-12-09 under 510(k) 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. The listed applicant is GE Medical Systems SCS. The 510(k) number is K251199.

When did Allia Moveo receive FDA 510(k) clearance?

Allia Moveo received FDA 510(k) clearance on 2025-12-09, under 510(k) number K251199.

Who is the listed applicant for Allia Moveo?

The FDA 510(k) record lists GE Medical Systems SCS as the applicant. This does not by itself establish the device manufacturer.

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.

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