IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND— 510(k) K024100
Substantially EquivalentTheratech, Inc.
FDA 510(k) clearance K024100 for IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND, Substantially Equivalent on 2003-02-25. Applicant: Theratech, Inc..
Clearance details
- Applicant
- Theratech, Inc.
- Product code
- Code LIH
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Taichung, TW
Data sourced from openFDA. This site is unofficial and independent of the FDA.