FDA applicant
Rescare, Ltd.
FDA records 5 decisions for Rescare, Ltd. (Findley, MN) from 1994 to 1996: 5 510(k) clearances. Most are in product codes BZD (Ventilator, Non-Continuous (Respirator)) and BTT (Humidifier, Respiratory Gas, (Direct Patient…). No recall is linked to its devices.
FDA’s records also spell it “Rescare, Inc.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Rescare, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Rescare, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Rescare, Ltd.’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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