Goosen Enterprises, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K923848 | GOOSEN SELF-LUBRICATING CATHETER | February 18, 1994 |
| K896134 | ACUFLO, VACUUM-POWERED BODY FLUID SUCTION APPARA. | August 30, 1990 |
| K896579 | GOOSEN URINARY DRAINAGE SYSTEM | February 15, 1990 |
| K844889 | MENSINK-GOOSEN CATHETER | March 18, 1985 |