FDA 510(k) Applications Submitted by Randy Parry
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K240408 | 02/09/2024 | REMI-AI Rapid Detection Module (REMI-AI RDM) | Epitel, Inc |
| K230933 | 04/03/2023 | REMI Remote EEG Monitoring System | Epitel, Inc. |
| K212372 | 07/30/2021 | Fitbit Irregular Rhythm Notifications | Fitbit Inc |
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