FDA 510(k) Applications Submitted by Jenny Hsieh

FDA 510(k) Number	Submission Date	Device Name	Applicant
K090023	01/05/2009	IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR, MODEL: WL-2206B AND WL-2106E	WELL-LIFE HEALTHCARE LIMITED
K080304	02/05/2008	PRO TENS, MODEL WL-240 RX	WELL-LIFE HEALTHCARE LIMITED
K220524	02/23/2022	Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)	Well-Life Healthcare Limited
K200942	04/08/2020	Well-Life Garment Electrodes (GM Series)	Well-Life Healthcare Limited
K091757	06/16/2009	OTC TENS FOR ARM AND LEG PAIN RELIEF, MODEL WL-2407	WELL-LIFE HEALTHCARE LIMITED
K072168	08/06/2007	OTC ABDOMEN & THIGH SYSTEM, MODEL: WL-2410, WL-2411 AND WL-2412	WELL-LIFE HEALTHCARE LIMITED
K222528	08/22/2022	Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/EMG Electrode Probe, Well-Life Probe Electrode	Well-Life Healthcare Limited
K092763	09/09/2009	IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D	WELL-LIFE HEALTHCARE LIMITED
K213091	09/24/2021	Well-Life TENS/EMS/Heating Stimulator	Well-Life Healthcare Limited
K102786	09/27/2010	WELL-LIFE OTC EMS SYSTEM	WELL-LIFE HEALTHCARE LIMITED
K063660	12/08/2006	OTC TENS FOR LOW BACK PAIN RELIEF, MODEL WL-2407	WELL-LIFE HEALTHCARE LIMITED