Class Class II

Allia Moveo (K251199)

K251199 2025-12-09 Traditional
Home/ Devices/ Allia Moveo (K251199)

Description

Allia Moveo by GE Medical Systems SCS, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251199
Clearance Date2025-12-09
Clearance TypeTraditional
Product CodeOWB
Regulation Number892.1650

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top