Covidien Lp, Formerly Registered AS Kendall
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K130725 | MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR. | April 17, 2013 |
| K112511 | DOBBHOFF DUAL PORT FEEDING TUBE | May 11, 2012 |
| K092205 | PALINDROME P HEMODIALYSIS CATHETER | October 30, 2009 |