Last synced on 14 November 2025 at 11:06 pm

LumiNE US; Lumi

Page Type
Cleared 510(K)
510(k) Number
K240094
510(k) Type
Traditional
Applicant
Augmedit B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
9/10/2024
Days to Decision
242 days
Submission Type
Summary

LumiNE US; Lumi

Page Type
Cleared 510(K)
510(k) Number
K240094
510(k) Type
Traditional
Applicant
Augmedit B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
9/10/2024
Days to Decision
242 days
Submission Type
Summary