Scandimed International
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K083556 | MODIFICATION TO AUTO-BAND LIGATOR | February 19, 2009 |
| K081142 | AUTO-BAND LIGATOR | May 16, 2008 |