# Cardinal Health 207, Inc.

- Location (FDA's records): Yorba Linda, CA
- FDA decisions: 5 (2008–2010): 5 510(k) clearances
- Product codes: CBK (3), BZD (1), BZR (1)
- Predicates its devices cite: 12 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bird Products Corp.: 3 (https://510kreport.com/company/bird-products)
- Tiara Medical Systems, Inc.: 2 (https://510kreport.com/company/tiara-medical-systems)
- Intersurgical, Inc.: 1 (https://510kreport.com/company/intersurgical)
- Resmed, Ltd.: 1 (https://510kreport.com/company/resmed)
- Precision Medical, Inc.: 1 (https://510kreport.com/company/precision-medical)
- Respironics, Inc.: 1 (https://510kreport.com/company/respironics)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Pulmonetic Systems, Inc.: 1 (https://510kreport.com/company/pulmonetic-systems)

## Firms that cite its devices most
- Covidien, Formerly Nellcor Puritan Bennett, Inc.: 1 (https://510kreport.com/company/covidien-formerly-nellcor-puritan-bennett)
- Care Fusion: 1 (https://510kreport.com/company/care-fusion)
- Telesair, Inc.: 1 (https://510kreport.com/company/telesair)

## Its most-cited devices
- K081837: Avea Ventilator (2008), cited by 2
- K093094: Vela Ventilator (2010), cited by 1

## Recent decisions
- K093094: Vela Ventilator (May 11, 2010)
- K092484: Heliox Low Flow Sentry Blender (Apr 2, 2010)
- K093124: Puresom Nasal Mask-Small, Puresom Nasal Mask-Medium, Puresom Nasal Mask-Large, Models 11924-01, 11924-02, 11924-03 (Mar 10, 2010)
- K081670: The Advantage Series Non-Vented (NV) Full Face Mask (Oct 9, 2008)
- K081837: Avea Ventilator (Aug 13, 2008)

Source page: https://510kreport.com/company/cardinal-health-207