Class Class II

HD+12, HD+15 (K220526)

K220526 2023-05-15 Traditional
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Description

HD+12, HD+15 by Cardioline S.P.A — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220526
Clearance Date2023-05-15
Clearance TypeTraditional
Product CodeDRG
Regulation Number870.2910

Categories

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