Rota Systems Medfurniture, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K935952 | ROTA SYSTEM 5000 | April 19, 1994 |
| K931839 | ROTA SYSTEM XL | November 22, 1993 |