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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
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