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Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie)

Page Type
Cleared 510(K)
510(k) Number
K222880
510(k) Type
Traditional
Applicant
Endolumik Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2023
Days to Decision
162 days
Submission Type
Summary

Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie)

Page Type
Cleared 510(K)
510(k) Number
K222880
510(k) Type
Traditional
Applicant
Endolumik Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2023
Days to Decision
162 days
Submission Type
Summary