FDA 510(k) Applications Submitted by Dymedix Diagnostics, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K200654 | 03/12/2020 | Rubicon SA System | Dymedix Diagnostics, Inc. |
| K192564 | 09/18/2019 | Disposable Gold Cup EEG Electrodes | Dymedix Diagnostics, Inc. |
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