FDA applicant
Kuschall of America
FDA records 4 decisions for Kuschall of America (Camarillo, CA) in 1995: 4 510(k) clearances. All are in product code IOR (Wheelchair, Mechanical). 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 Kuschall of America’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kuschall of America since 2007.
Recalls per year
No recall linked to its devices since 2007.
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