Class Class II

Babylog VN800, Babylog VN600 (K222207)

K222207 2023-05-16 Traditional
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Description

Babylog VN800, Babylog VN600 by Draegerwerk AG & CO Kgaa — FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222207
Clearance Date2023-05-16
Clearance TypeTraditional
Product CodeCBK
Regulation Number868.5895

Categories

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