FDA applicant
Skil-Care Corp.
FDA records 20 decisions for Skil-Care Corp. (Yonkers, NY) from 1979 to 2001: 20 510(k) clearances. Most are in product codes FMQ (Restraint, Protective) and KID (Restraint, Wheelchair, Non-Protective). 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 Skil-Care Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Skil-Care Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Skil-Care Corp.’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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