Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)— 510(k) K220524
Substantially EquivalentWell-Life Healthcare Limited
FDA 510(k) clearance K220524 for Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series), Substantially Equivalent on 2022-08-04. Applicant: Well-Life Healthcare Limited. Device class: 2.
Clearance details
- 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
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Data sourced from openFDA. This site is unofficial and independent of the FDA.