K-number	K162622
Device name	Fujifilm Endoscope Models EC-600HL and EC-600LS
Applicant	Fujifilm Medical Systems U.S.A, Inc.
Product code	FDF
Device class	Class II
Decision date	Oct 18, 2016
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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Fujifilm Endoscope Models EC-600HL and EC-600LS

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