Pfm Produkte Fur Die Medizin AG
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K011783 | MULTI-SNARE SET | January 24, 2002 |
| K002471 | JETCAN HUBER NEEEDLE SET | October 19, 2000 |
| K001716 | REDON SET | July 19, 2000 |