Class Class II

AccurECG Analysis System (v2.0) (K252361)

K252361 2025-12-22 Traditional
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Description

AccurECG Analysis System (v2.0) by Accurkardia, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252361
Clearance Date2025-12-22
Clearance TypeTraditional
Product CodeDPS
Regulation Number870.2340

Categories

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