Cardinal Health, Alaris Products
San Diego, CA, US
Cardinal Health, Alaris Products appears in FDA device records in San Diego, CA. FDA records list 9 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Cardinal Health, Alaris Products between 2005 and 2007. The busiest year on record is 2005, with 5. The most recent is 2007, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2005 | 5 |
| 2006 | 2 |
| 2007 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K071400 | SMARTSITE STOPCOCK | FMG | Substantially Equivalent | |
| K071108 | TEXIUM SYRINGE | FMF | Substantially Equivalent | |
| K061285 | SMARTSITE NEEDLE FREE VALVE ADMINISTRATION SETS | FPA | Substantially Equivalent | |
| K053049 | ALARIS SAFETY MALE LUER | FPA | Substantially Equivalent | |
| K052790 | SMARTSITE VENTED VIAL ACCESS DEVICE, MODEL TBD | LHI | Substantially Equivalent | |
| K051641 | ALARIS SYSTEM PC UNIT, MODEL 8001 | FRN | Substantially Equivalent | |
| K050115 | BLOOD HAND PUMP ADMINISTRATION SET | BRZ | Substantially Equivalent | |
| K043590 | SE INFUSION SYSTEM WITH MMS | FRN | Substantially Equivalent | |
| K050230 | TURBO TEMP TRIO | FLL | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain