Class Class II

KabiHelp® Uno; KabiHelp® Advance plus (K251139)

K251139 2026-01-09 Traditional
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Description

KabiHelp® Uno; KabiHelp® Advance plus by Fresenius Kabi AG, an FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251139
Clearance Date2026-01-09
Clearance TypeTraditional
Product CodeKPE
Regulation Number880.5025

Categories

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