Rochester Electro Medical, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K142159 | DISPOSABLE PRE-GELLED SURFACE ELECTRODE | June 3, 2015 |
| K080914 | ULTRASHARP CONCENTRIC NEEDLES | July 15, 2008 |