K-number	K213925
Device name	MyoCycle MC-2 (Home / Home + / Pro / Pro +)
Applicant	Myolyn, LLC
Product code	GZI
Device class	Class II
Decision date	Apr 25, 2022
Decision	Substantially Equivalent
Regulation	882.5810

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View the full FDA submission: accessdata.fda.gov

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MyoCycle MC-2 (Home / Home + / Pro / Pro +)

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