Berchtold GmbH & Co. KG
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K120392 | CHROMOPHARE F 628 AND F 528 | February 16, 2012 |
| K090378 | CHROMOPHARE E 668 | February 23, 2009 |