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DiLumen Endolumenal Interventional Platform

Page Type
Cleared 510(K)
510(k) Number
K182540
510(k) Type
Traditional
Applicant
Lumendi, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2018
Days to Decision
46 days
Submission Type
Summary

DiLumen Endolumenal Interventional Platform

Page Type
Cleared 510(K)
510(k) Number
K182540
510(k) Type
Traditional
Applicant
Lumendi, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2018
Days to Decision
46 days
Submission Type
Summary