Company ยท US
Cardinal Health, Alaris Products
FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2007. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Dec 14, 2007 | K071400 | SMARTSITE STOPCOCK Cardinal Health, Alaris Products | FMG |
| May 24, 2007 | K071108 | TEXIUM SYRINGE Cardinal Health, Alaris Products | FMF |
| Jul 26, 2006 | K061285 | SMARTSITE NEEDLE FREE VALVE ADMINISTRATION SETS Cardinal Health, Alaris Products | FPA |
| Jan 12, 2006 | K053049 | ALARIS SAFETY MALE LUER Cardinal Health, Alaris Products | FPA |
| Dec 23, 2005 | K052790 | SMARTSITE VENTED VIAL ACCESS DEVICE, MODEL TBD Cardinal Health, Alaris Products | LHI |
| Oct 20, 2005 | K051641 | ALARIS SYSTEM PC UNIT, MODEL 8001 Cardinal Health, Alaris Products | FRN |
| Apr 1, 2005 | K050115 | BLOOD HAND PUMP ADMINISTRATION SET Cardinal Health, Alaris Products | BRZ |
| Mar 25, 2005 | K043590 | SE INFUSION SYSTEM WITH MMS Cardinal Health, Alaris Products | FRN |
| Feb 16, 2005 | K050230 | TURBO TEMP TRIO Cardinal Health, Alaris Products | FLL |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||