Data / Medical devices / Colombia / Cardinal Health Colombia S.A.S.
Cardinal Health Colombia S.A.S.: FDA-registered device maker in Bogota, Colombia, 1 510(k) clearance
Cardinal Health Colombia S.A.S. is registered with the FDA (registration 3014110920) in Bogota, Colombia. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 27, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014110920
- Address
- Carrera 7 No. 116 - 50, Piso 5., Bogota, Colombia, 999998
- Owner or operator
- Cardinal Health 200, LLC (9028292)
- Roles
- Exporter to the US
- First device listed
- July 27, 2018
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Sleeve, Limb, Compressible | JOW | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| August 27, 2013 | K132360 | KENDALL SCD 700 SEQUENTIAL COMPRESSION CONTROLLER | JOW | Substantially Equivalent | Covidien | accessdata.fda.gov |
Compare with other makers
Updated August 27, 2013. 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.