Alfa Tech Medical Systems, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K063728 | TNN-DU810 NON-INVASIVE SUBDERMAL THERAPY SYSTEM | April 4, 2007 |
| K052340 | DU857 DUAL FREQUENCY ULTRASOUND THERAPY AND MUSCLE STIMULATOR SYSTEM | December 9, 2005 |