Last synced on 14 November 2025 at 11:06 pm

NEXUS TKO-6P LUER ACTIVATED DEVICE

Page Type
Cleared 510(K)
510(k) Number
K130416
510(k) Type
Traditional
Applicant
NEXUS MEDICAL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2013
Days to Decision
113 days
Submission Type
Statement

NEXUS TKO-6P LUER ACTIVATED DEVICE

Page Type
Cleared 510(K)
510(k) Number
K130416
510(k) Type
Traditional
Applicant
NEXUS MEDICAL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2013
Days to Decision
113 days
Submission Type
Statement