K-number	K202130
Device name	FUJIFILM Video Laparoscope
Applicant	Fujifilm Corporation
Product code	GCJ
Device class	Class II
Decision date	Aug 20, 2020
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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FUJIFILM Video Laparoscope

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