FDA FDA 510(k) clearance: Santreva-ATK Endovascular Revasculariztion Catheter — K252315, Sep 22, 2025. Applicant at approval: AngioSafe, Inc. source ↗
FDA records (last 2 years)
FDA 510(k) clearance: Santreva-ATK Endovascular Revasculariztion Catheter — K252315, Sep 22, 2025. Applicant at approval: AngioSafe, Inc. source ↗
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