Electromedical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K903014 | ALPHA-STIM CS | May 12, 1992 |
| K896948 | ALPHA-STIM CS | February 23, 1990 |
| K881753 | ALPHA-STIM 350 | August 30, 1988 |
| K831145 | ALPHA-STIM 350 | July 7, 1983 |
| K831144 | ALPHA-STIM 2000 | June 30, 1983 |