Class Class II

FEops HEARTguide Simulation Application (K250635)

K250635 2025-11-25 Traditional
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Description

FEops HEARTguide Simulation Application by Feops NV, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250635
Clearance Date2025-11-25
Clearance TypeTraditional
Product CodeQQI
Regulation Number870.1405

Categories

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