K-number	K161204
Device name	ENDOCAM Flex HD Camera System 5521
Applicant	Richard Wolf Medical Instruments Corporation
Product code	FET
Device class	Class II
Decision date	Jan 11, 2017
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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ENDOCAM Flex HD Camera System 5521

Everything you need for a 510(k) submission. Nothing you don't.