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Luminelle DTx Hysteroscopy System

Page Type
Cleared 510(K)
510(k) Number
K181909
510(k) Type
Traditional
Applicant
UVision360 Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2018
Days to Decision
30 days
Submission Type
Summary

Luminelle DTx Hysteroscopy System

Page Type
Cleared 510(K)
510(k) Number
K181909
510(k) Type
Traditional
Applicant
UVision360 Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2018
Days to Decision
30 days
Submission Type
Summary