FDA 510(k) Applications Submitted by Hi-Dow International, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K233461 | 10/23/2023 | Hi-Dow PRO TOUCH WIRELESS 6-12 (HD-19A) | Hi-Dow International, Inc. |
| K163393 | 12/02/2016 | Hi-Dow Wireless TENS/EMS System (Model HD-5N) | Hi-Dow International, Inc. |
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