Class Class II

Azurion R3.1 (K254186)

K254186 2026-01-16 Special
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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) NumberK254186
Clearance Date2026-01-16
Clearance TypeSpecial
Product CodeOWB
Regulation Number892.1650

Categories

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