Class Class II

Alphenix, INFX-8000V/B, INFX-8000V/S, V9.5 (K233107)

K233107 2024-08-30 Traditional
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Description

Alphenix, INFX-8000V/B, INFX-8000V/S, V9.5 by Canon Medical Systems Corporation — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK233107
Clearance Date2024-08-30
Clearance TypeTraditional
Product CodeOWB
Regulation Number892.1650

Categories

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