Class Class II

ArteVu (K244007)

K244007 2025-07-30 Traditional
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Description

ArteVu by Cardio Ring Technologies, Inc. Taiwan Branch, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK244007
Clearance Date2025-07-30
Clearance TypeTraditional
Product CodeDXN
Regulation Number870.1130

Categories

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