K-number	K170132
Device name	MyoCycle Home, MyoCycle Pro
Applicant	Myolyn, LLC
Product code	GZI
Device class	Class II
Decision date	Apr 25, 2017
Decision	Substantially Equivalent
Regulation	882.5810

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Source

View the full FDA submission: accessdata.fda.gov

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MyoCycle Home, MyoCycle Pro

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