Class Class II

LAIA XR (K251577)

K251577 2026-02-06 Traditional
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Description

LAIA XR by Augmented Reality Software S.L., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251577
Clearance Date2026-02-06
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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