FDA 510(k)

Allia Moveo

K号: K251199 · 2025-12-09

决定日期2025-12-09

产品代码OWB

咨询委员会RA

决定实质等同

器械摘要

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.

常见问题

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?

FDA 510(k)记录列出了GE医疗系统SCS为申请人。这本身并不能确立该设备制造商。

What is the FDA product code for Allia Moveo?

The FDA product code for Allia Moveo is OWB.

列明GE Medical Systems SCS为申报人的其他记录

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