Hennig Enterprises Europe Srl
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K020424 | V SET | August 29, 2003 |
| K020421 | GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES | April 29, 2003 |