Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/EMG Electrode Probe, Well-Life Probe Electrode— 510(k) K222528
Substantially EquivalentWell-Life Healthcare Limited
FDA 510(k) clearance K222528 for Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/EMG Electrode Probe, Well-Life Probe Electrode, Substantially Equivalent on 2022-12-29. Applicant: Well-Life Healthcare Limited. Device class: 2.
Clearance details
- Applicant
- Well-Life Healthcare Limited
- Product code
- Code KPI
- Device class
- Class 2
- Regulation
- 21 CFR 876.5320
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Taipei City, TW
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More clearances from Well-Life Healthcare Limited
view allData sourced from openFDA. This site is unofficial and independent of the FDA.