Shenzhen Kentro Medical Electronics Co., Ltd.
Shenzhen Kentro Medical Electronics Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2024.
Top product codes for Shenzhen Kentro Medical Electronics Co., Ltd.
Recent clearances by Shenzhen Kentro Medical Electronics Co., Ltd.
- K242332 — 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)
- K232517 — Transcutaneous Electrical Nerve Stimulator For Pain Relief (Model: KTR-2302, KTR-2401, KTR-2402, KTR-2411, KTR-2412)
- K222870 — 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
- K220998 — Transcutaneous Electrical Nerve Stimulator, Model: KTR-405
- K200177 — Low-frequency Multi-function physiotherapy instrument
- K200237 — Transcutaneous Electronic Nerve Stimulator
- K191982 — 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)
- K183288 — Transcutaneous Electrical Nerve Stimulator
- K181728 — Muscle Trainer
- K170205 — Low-Frequency Therapy Instrument /Model: KTR-201, KTR-202, KTR-203
Data sourced from openFDA. This site is unofficial and independent of the FDA.