Well-Life Healthcare Limited
FDA 510(k) medical device clearances.
Top product codes for Well-Life Healthcare Limited
Recent clearances by Well-Life Healthcare Limited
- K233054 — Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator; TENS/EMS WITH Menstrual Relief Stimulator; Well-Life Pain Relief Stimulator; Menstrual Plus Stimulator
- K222528 — Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/EMG Electrode Probe, Well-Life Probe Electrode
- K220524 — Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)
- K213091 — Well-Life TENS/EMS/Heating Stimulator
- K200942 — Well-Life Garment Electrodes (GM Series)
- K172809 — OTC Combo TENS/EMS System
- K162663 — WELL LIFE Rx Wireless TENS/EMS Stimulator, model WR-2603/2603A, WR-2604/2604A and WR-2605/2605A
- K161453 — WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A
- K141299 — OTC COMBO TENS/EMS SYSTEM
- K133723 — OTC PATCH
- K123075 — BUTTOCK MUSCLE STIMULATOR MODEL WL-2413B; BUTTOCK MUSCLE STIMULATOR MODE WL-2413E
- K121353 — MINI PATCH
- K102786 — WELL-LIFE OTC EMS SYSTEM
- K100399 — 4 CHANNELS MULTIPLE MODEL DIGITAL ELECTRICAL STIMULATOR, MODEL NUVOSTIM IV, WL-2504A
- K091757 — OTC TENS FOR ARM AND LEG PAIN RELIEF, MODEL WL-2407
- K092763 — IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D
- K082065 — WELL LIFE SELF ADHESIVE ELECTRODE / MODELS: CM, FA, PU AND SP
- K090023 — IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR, MODEL: WL-2206B AND WL-2106E
- K080304 — PRO TENS, MODEL WL-240 RX
- K072168 — OTC ABDOMEN & THIGH SYSTEM, MODEL: WL-2410, WL-2411 AND WL-2412
- K063660 — OTC TENS FOR LOW BACK PAIN RELIEF, MODEL WL-2407
- K052785 — OTC TENS FOR LOW BACK PAIN RELIEF, MODEL WL-2405 AND WL-2406
Data sourced from openFDA. This site is unofficial and independent of the FDA.