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DiLumen Endolumenal Interventional Platform

Page Type
Cleared 510(K)
510(k) Number
K162428
510(k) Type
Traditional
Applicant
Lumendi, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2016
Days to Decision
98 days
Submission Type
Summary

DiLumen Endolumenal Interventional Platform

Page Type
Cleared 510(K)
510(k) Number
K162428
510(k) Type
Traditional
Applicant
Lumendi, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2016
Days to Decision
98 days
Submission Type
Summary