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DiLumen Endolumenal Interventional Platform (DiLumen)

Page Type
Cleared 510(K)
510(k) Number
K210851
510(k) Type
Special
Applicant
Lumendi, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2021
Days to Decision
30 days
Submission Type
Summary

DiLumen Endolumenal Interventional Platform (DiLumen)

Page Type
Cleared 510(K)
510(k) Number
K210851
510(k) Type
Special
Applicant
Lumendi, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2021
Days to Decision
30 days
Submission Type
Summary