Class Class II

vWF Ag (K220728)

K220728 2023-06-02 Traditional
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Description

vWF Ag by Siemens Healthcare Diagnostics Products GmbH — FDA 510(k) cleared hematology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220728
Clearance Date2023-06-02
Clearance TypeTraditional
Product CodeGGP
Regulation Number864.7290

Categories

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