Class Class II

Volumat Line (K220301)

K220301 2023-06-02 Traditional
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Description

Volumat Line by Fresenius Kabi — FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220301
Clearance Date2023-06-02
Clearance TypeTraditional
Product CodeFPA
Regulation Number880.5440

Categories

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