Class Class II

Vivo 45 LS (K232365)

K232365 2025-12-19 Traditional
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Description

Vivo 45 LS by Oconnell Regulatory Consultants, Inc., an FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK232365
Clearance Date2025-12-19
Clearance TypeTraditional
Product CodeCBK
Regulation Number868.5895

Categories

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