Class Class II

syngo.via View&GO VA40A (K230196)

K230196 2023-02-13 Traditional
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Description

syngo.via View&GO VA40A by Siemens Healthcare GmbH — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230196
Clearance Date2023-02-13
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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