Yukon Medical, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K240761Arisure® Closed Male Luer with Spike Adapter (YM060)March 21, 2025
K243486SmartSiteTM Vented Vial Access DeviceDecember 6, 2024
K201422Arisure Closed System Drug Transfer Device (CSTD)March 2, 2021
K172884Arisure Closed Vial AdapterOctober 3, 2017
K172631Arisure Dry SpikeSeptember 29, 2017
K171101Closed Male LuerJune 2, 2017
K151963SmartSite Vented Vial Access DeviceJuly 31, 2015
K132863SMARTSITE VIALSHIELDOctober 4, 2013
K122265VIALOK SINGLE VIAL ACCESS DEVICE VENTEDAugust 14, 2012
K121182VIALOK NON-VENTEDMay 3, 2012
K120799ARISURE NEUTRAL VALVEMarch 30, 2012