FDA applicant
Cardinal Health 207, Inc.
FDA records 5 decisions for Cardinal Health 207, Inc. (Yorba Linda, CA) from 2008 to 2010: 5 510(k) clearances. Most are in product codes CBK (Ventilator, Continuous, Facility Use) and BZD (Ventilator, Non-Continuous (Respirator)). Its devices cite 12 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Cardinal Health 207, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
3in 2010
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2008.
Planning a device like Cardinal Health 207, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Cardinal”
FDA records each applicant name separately; these may or may not be the same firm.