Yukon Medical

Timeline

1. Mar 21, 2025 FDA FDA 510(k) clearance: Arisure® Closed Male Luer with Spike Adapter (YM060) — K240761, Mar 21, 2025. Applicant at approval: Yukon Medical, LLC. source ↗
2. Dec 6, 2024 FDA FDA 510(k) clearance: SmartSiteTM Vented Vial Access Device — K243486, Dec 6, 2024. Applicant at approval: Yukon Medical, LLC. source ↗

FDA records (last 2 years)

• Mar 21, 2025 FDA 510(k) clearance: Arisure® Closed Male Luer with Spike Adapter (YM060) — K240761, Mar 21, 2025. Applicant at approval: Yukon Medical, LLC. source ↗
• Dec 6, 2024 FDA 510(k) clearance: SmartSiteTM Vented Vial Access Device — K243486, Dec 6, 2024. Applicant at approval: Yukon Medical, LLC. source ↗