FDA applicant
E. Benson Hood Laboratories, Inc.
FDA records 6 decisions for E. Benson Hood Laboratories, Inc. (Mchenry, IL) from 1984 to 1999: 6 510(k) clearances. Most are in product codes BTO (Tube, Tracheostomy (W/Wo Connector)) and FWN (Prosthesis, Larynx (Stents And Keels)). 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 E. Benson Hood Laboratories, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for E. Benson Hood Laboratories, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like E. Benson Hood Laboratories, Inc.’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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