FDA applicant
Kurt Mfg. Co.
FDA records 1 decision for Kurt Mfg. Co. (Minneapolis, MN) in 1999: 1 510(k) clearance. All are in product code ITI (Wheelchair, Powered). 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 Kurt Mfg. Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kurt Mfg. Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Kurt Mfg. Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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