Unique Flotation Systems, 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 |
|---|
| K904008 | STAGE IV, AIR-FLUIDIZE BED | October 10, 1990 |
| K903659 | STAGE III | September 17, 1990 |