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NEXUS TKO-6, LUER-ACTIVATED DEVICE

Page Type
Cleared 510(K)
510(k) Number
K113398
510(k) Type
Traditional
Applicant
NEXUS MEDICAL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2012
Days to Decision
153 days
Submission Type
Statement

NEXUS TKO-6, LUER-ACTIVATED DEVICE

Page Type
Cleared 510(K)
510(k) Number
K113398
510(k) Type
Traditional
Applicant
NEXUS MEDICAL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2012
Days to Decision
153 days
Submission Type
Statement