FDA applicant
Churchill Corp.
FDA records 35 decisions for Churchill Corp. (Langhorne, PA) from 1985 to 1988: 35 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FPK (Tubing, Fluid Delivery). 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 Churchill Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Churchill Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Churchill Corp.’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 “Churchill”
FDA records each applicant name separately; these may or may not be the same firm.