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. |
| K242332 |
08/07/2024 |
Transcutaneous Electronic Nerve Stimulator (KTR-2301, KTR-2302, KTR-2341, KTR-2342, KTR-2401, KTR-2402, KTR-2411, KTR-2412, KTR-2491, KTR-2492, KTR-2493, KTR-2494) |
Shenzhen Kentro Medical Electronics Co., Ltd. |
| K232517 |
08/18/2023 |
Transcutaneous Electrical Nerve Stimulator For Pain Relief (Model: KTR-2302, KTR-2401, KTR-2402, KTR-2411, KTR-2412) |
Shenzhen Kentro Medical Electronics Co., Ltd. |
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