FDA 510(k) Applications Submitted by MYOLYN, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170132 | 01/17/2017 | MyoCycle Home, MyoCycle Pro | MYOLYN, LLC |
| K213925 | 12/16/2021 | MyoCycle MC-2 (Home / Home + / Pro / Pro +) | Myolyn, LLC |
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