Cardinal Health, Alaris Products
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K071400 | SMARTSITE STOPCOCK | December 14, 2007 |
| K071108 | TEXIUM SYRINGE | May 24, 2007 |
| K061285 | SMARTSITE NEEDLE FREE VALVE ADMINISTRATION SETS | July 26, 2006 |
| K053049 | ALARIS SAFETY MALE LUER | January 12, 2006 |
| K052790 | SMARTSITE VENTED VIAL ACCESS DEVICE, MODEL TBD | December 23, 2005 |
| K051641 | ALARIS SYSTEM PC UNIT, MODEL 8001 | October 20, 2005 |
| K050115 | BLOOD HAND PUMP ADMINISTRATION SET | April 1, 2005 |
| K043590 | SE INFUSION SYSTEM WITH MMS | March 25, 2005 |
| K050230 | TURBO TEMP TRIO | February 16, 2005 |