Class Class II

AI-CVD (K252029)

K252029 2025-12-19 Traditional
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Description

AI-CVD by HeartLung Corporation, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252029
Clearance Date2025-12-19
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050

Categories

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