Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator +3 more— 510(k) K233054
Substantially EquivalentWell-Life Healthcare Limited
FDA 510(k) clearance K233054 for Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator +3 more, Substantially Equivalent on 2024-10-18. Applicant: Well-Life Healthcare Limited. Device class: 2.
Clearance details
- Device name as filed
- Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator; TENS/EMS WITH Menstrual Relief Stimulator; Well-Life Pain Relief Stimulator; Menstrual Plus Stimulator
- Applicant
- Well-Life Healthcare Limited
- Product code
- Code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Taipei City, TW
Recent devices under product code NUH
view all- K261131 — Electrical Muscle Stimulator (AST-105DJ, AST-105EJ, AST- 105BJ, AST-105GJ, AST-303J, AST-309J, AST-310J +6 more
- K260412 — TENS 7000 Rechargeable 4 Channel (TENS 7000H)
- K260425 — TENS / EMS DEVICE (FT-247 Series) (FT-247, FT-237)
- K253896 — TENS/EMS device (GUSE01)
- K253305 — TENS AND EMS (TENS and Muscle Stimulator) (JT1065, JT1080, JT2080, JT9034)
More clearances from Well-Life Healthcare Limited
view all- 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
Data sourced from openFDA. This site is unofficial and independent of the FDA.