Data / Medical devices / United States / Cardinal Health 200, LLC
Cardinal Health 200, LLC: FDA-registered device maker in Jacksonville, TX, United States, 1 510(k) clearance
Cardinal Health 200, LLC is registered with the FDA (registration 1623486) in Jacksonville, TX, United States. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 9, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1623486
- Address
- 200 Mcknight ST., Jacksonville, TX, United States, 75766
- Owner or operator
- Cardinal Health 200, LLC (9028292)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- August 3, 1995
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suction, Operating-Room, Wall Vacuum Powered | GCX | 2 | Manufacturer | accessdata.fda.gov |
| Apparatus, Suction, Single Patient Use, Portable, Nonpowered | GCY | 1 | Manufacturer | accessdata.fda.gov |
| Basin, Emesis | FNY | 1 | Manufacturer | accessdata.fda.gov |
| Container, Liquid Medication, Graduated | KYW | 1 | Manufacturer | accessdata.fda.gov |
| Container, Specimen Mailer And Storage, Sterile | KDT | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Contract manufacturer | accessdata.fda.gov |
| Stand, Infusion | FOX | 1 | Manufacturer | accessdata.fda.gov |
| Tubes, Gastrointestinal (And Accessories) | KNT | 2 | Manufacturer | accessdata.fda.gov |
| Tubing, Pressure And Accessories | BYX | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 9, 2014 | K123555 | KANGAROO FEEDING TUBES WITH IRIS TECHNOLOGY | KNT | Substantially Equivalent | Covidien | accessdata.fda.gov |
Compare with other makers
- All makers of Basin, Emesis
- All makers of Apparatus, Suction, Single Patient Use, Portable, Nonpowered
- All makers of Container, Liquid Medication, Graduated
- All makers of Tubing, Pressure And Accessories
- All makers of Stand, Infusion
- All makers of Container, Specimen Mailer And Storage, Sterile
Updated April 9, 2014. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.