Class Class II

SureAx-Guide™ (K250203)

K250203 2025-10-17 Traditional
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Description

SureAx-Guide™ by Sureax Medical, LLC, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250203
Clearance Date2025-10-17
Clearance TypeTraditional
Product CodeDQX
Regulation Number870.1330

Categories

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