Class Class II

Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie) (K222880)

K222880 2023-03-03 Traditional
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Description

Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie) by Endolumik, Inc. — FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222880
Clearance Date2023-03-03
Clearance TypeTraditional
Product CodeKNT
Regulation Number876.5980

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