FDA 510(k) Applications Submitted by Shenzhen Kentro Medical Electronics Co., Ltd
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K170205 |
01/23/2017 |
Low-Frequency Therapy Instrument /Model: KTR-201, KTR-202, KTR-203 |
Shenzhen Kentro Medical Electronics Co., Ltd |
| K200177 |
01/24/2020 |
Low-frequency Multi-function physiotherapy instrument |
Shenzhen Kentro Medical Electronics Co., Ltd |
| K200237 |
01/24/2020 |
Transcutaneous Electronic Nerve Stimulator |
Shenzhen Kentro Medical Electronics Co., Ltd |
| K181728 |
06/29/2018 |
Muscle Trainer |
Shenzhen Kentro Medical Electronics Co., Ltd |
| K191982 |
07/25/2019 |
Low-Frequency Multi-function Physiotherapy Instrument (Model: KTR-2230, KTR-2220, KTR-2210, KTR-2231, KTR-2221, KTR-2211, KTR-2232, KTR-2222, KTR-2212) |
Shenzhen Kentro Medical Electronics Co., Ltd |
| K222870 |
09/22/2022 |
Transcutaneous Electrical Nerve Stimulator, Model: KTR-4031, KTR-4032, KTR-4012, KTR-4015, KTR-4029, KTR-4027, KTR-4026, KTR-4021, KTR-4034, KTR-4036, KTR-4037, KTR-4039 |
Shenzhen Kentro Medical Electronics Co., Ltd |
| K183288 |
11/26/2018 |
Transcutaneous Electrical Nerve Stimulator |
Shenzhen Kentro Medical Electronics Co., Ltd |
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