B. Braun Medizintechnologie GmbH
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K072760 | SOLCART B | January 29, 2008 |
| K071518 | DIACAP LO PS (10, 12, 15) AND DIACAP HI PS (10, 12, 15, 18, 20) HEMODIALYZERS | August 17, 2007 |
| K052764 | DIACAP ULTRA DIALYSIS FLUID FILTER | June 9, 2006 |