IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR, MODEL: WL-2206B AND WL-2106E— 510(k) K090023
Substantially EquivalentWell-Life Healthcare Limited
FDA 510(k) clearance K090023 for IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR, MODEL: WL-2206B AND WL-2106E, Substantially Equivalent on 2009-01-30. Applicant: Well-Life Healthcare Limited. Device class: 2.
Clearance details
- Applicant
- Well-Life Healthcare Limited
- Product code
- Code LIH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Yunghe City, Taipei County, TW
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Data sourced from openFDA. This site is unofficial and independent of the FDA.