Activator Methods International, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K112606 | ACTIVATOR V-E | March 6, 2012 |
| K072519 | ACTIVATOR V SPINAL ADJUSTING INSTRUMENT | October 23, 2007 |
| K003185 | FS ACTIVATOR III | March 20, 2001 |