GEMORE TRUE SINE INTERFERENTIAL STIMULATOR— 510(k) K122944
Substantially EquivalentGemore Technology Co, Ltd.
FDA 510(k) clearance K122944 for GEMORE TRUE SINE INTERFERENTIAL STIMULATOR, Substantially Equivalent on 2012-12-21. Applicant: Gemore Technology Co, Ltd..
Clearance details
- Applicant
- Gemore Technology Co, Ltd.
- Product code
- Code LIH
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Tan Shui, New Taipei City, TW
Data sourced from openFDA. This site is unofficial and independent of the FDA.