Williams Specialty Products, 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 |
|---|
| K900641 | CANNULA, SUCTION UTERINE | March 30, 1990 |
| K900642 | SWIVEL ADAPTER | March 19, 1990 |