Class Class II

Model 9160 VitaloQUB (K223818)

K223818 2023-05-25 Traditional
Home/ Devices/ Model 9160 VitaloQUB (K223818)

Description

Model 9160 VitaloQUB by Vitalograph Ireland, Ltd. — FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223818
Clearance Date2023-05-25
Clearance TypeTraditional
Product CodeJEH
Regulation Number868.1760

Categories

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