Huntleigh Diagnostics , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K020390 | MODIFICATION TO FETAL ASSIST | April 19, 2002 |
| K002548 | FETAL ASSIST | March 6, 2001 |
| K001677 | BABY DOPPLEX 4000 (BD4000) | August 14, 2000 |