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MyoCycle Home, MyoCycle Pro

Page Type
Cleared 510(K)
510(k) Number
K170132
510(k) Type
Traditional
Applicant
MYOLYN, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2017
Days to Decision
98 days
Submission Type
Summary

MyoCycle Home, MyoCycle Pro

Page Type
Cleared 510(K)
510(k) Number
K170132
510(k) Type
Traditional
Applicant
MYOLYN, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2017
Days to Decision
98 days
Submission Type
Summary