Medical Flotation Systems, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K893801 | M.F.S. LOW AIR LOSS PULSATING BED | July 25, 1989 |
| K890200 | PNEUMATIC DORSIFLEXOR | February 3, 1989 |
| K884907 | BUMPY MEDICAL MASSAGE MAT | December 27, 1988 |
| K884908 | ULTRAFLOTATION MEDICAL WHEELCHAIR | December 27, 1988 |
| K882607 | ULTRAFLOTATION BED | October 14, 1988 |