Class Class II

Santreva™-ATK Endovascular Revasculariztion Catheter (K252315)

K252315 2025-09-22 Traditional
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Description

Santreva™-ATK Endovascular Revasculariztion Catheter by AngioSafe, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252315
Clearance Date2025-09-22
Clearance TypeTraditional
Product CodePDU
Regulation Number870.1250

Categories

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