Class Class II

CardioTag™ (K243566)

K243566 2025-07-22 Traditional
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Description

CardioTag™ by Cardiosense, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243566
Clearance Date2025-07-22
Clearance TypeTraditional
Product CodeDXR
Regulation Number870.2320

Categories

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