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SmartSite Vented Vial Access Device

Page Type
Cleared 510(K)
510(k) Number
K151963
510(k) Type
Traditional
Applicant
YUKON MEDICAL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2015
Days to Decision
15 days
Submission Type
Summary

SmartSite Vented Vial Access Device

Page Type
Cleared 510(K)
510(k) Number
K151963
510(k) Type
Traditional
Applicant
YUKON MEDICAL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2015
Days to Decision
15 days
Submission Type
Summary