Electro-Diagnostic Imaging, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K003442 | MODIFICATION TO EDI VERIS SYSTEM | May 4, 2001 |
| K983983 | EDI VERIS SYSTEM | February 3, 1999 |