FDA 510(k) Applications Submitted by Shenzhen Kentro Medical Electronics Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220998 | 04/04/2022 | Transcutaneous Electrical Nerve Stimulator, Model: KTR-405 | Shenzhen Kentro Medical Electronics Co., Ltd. |
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