Hankscraft Div. of Gerber Products Co.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K844013 | CARE ELECTRIC BREAST PUMP | February 15, 1985 |
| K790966 | ULTRASONIC HUMIDIFIER | June 11, 1979 |