Class Class II

Artix BG (K223000)

K223000 2023-01-11 Traditional
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Description

Artix BG by Inari Medical — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223000
Clearance Date2023-01-11
Clearance TypeTraditional
Product CodeQEW
Regulation Number870.5150

Categories

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