Florida Medical Industries, 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 |
| K964523 | RECOVER INFANT HEEL WARMER (5100) | February 10, 1997 |
| K963689 | RECOVER ADULT VEIN WARMER | December 12, 1996 |