Class Class II

Azurion R3.1 (K251827)

K251827 2025-10-24 Traditional
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Description

Azurion R3.1 by Philips Medical Systems B.V., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251827
Clearance Date2025-10-24
Clearance TypeTraditional
Product CodeOWB
Regulation Number892.1650

Categories

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