Shenzhen Kentro Medical Electronics Co., Ltd.
FDA 510(k) medical device clearances.
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.