K-number	K162330
Device name	Flex Robotic System and Flex Colorectal Drive
Applicant	Medrobotics Corporation
Product code	FDF
Device class	Class II
Decision date	May 4, 2017
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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Flex Robotic System and Flex Colorectal Drive

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