K-number	K171096
Device name	Fujifilm Diathermic Slitter (FlushKnife)
Applicant	Fujifilm Medical Systems U.S.A, Inc.
Product code	KGE
Device class	Class II
Decision date	May 9, 2017
Decision	Substantially Equivalent
Regulation	876.4300

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View the full FDA submission: accessdata.fda.gov

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Fujifilm Diathermic Slitter (FlushKnife)

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