K-number	K173405
Device name	DiLumen Endolumenal Interventional Scissors (DiLumen Is)
Applicant	Lumendi, LLC
Product code	GEI
Device class	Class II
Decision date	May 22, 2018
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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DiLumen Endolumenal Interventional Scissors (DiLumen Is)

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