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NEXUS NIS-6P LUER ACTIVATED DEVICE

Page Type
Cleared 510(K)
510(k) Number
K133351
510(k) Type
Traditional
Applicant
NEXUS MEDICAL LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2014
Days to Decision
203 days
Submission Type
Summary

NEXUS NIS-6P LUER ACTIVATED DEVICE

Page Type
Cleared 510(K)
510(k) Number
K133351
510(k) Type
Traditional
Applicant
NEXUS MEDICAL LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2014
Days to Decision
203 days
Submission Type
Summary