FDA applicant
B & F Medical Products, Inc.
FDA records 18 decisions for B & F Medical Products, Inc. (Mchenry, IL) from 1976 to 1994: 18 510(k) clearances. Most are in product codes BYG (Mask, Oxygen) and CAW (Generator, Oxygen, Portable). 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 B & F Medical Products, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for B & F Medical Products, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like B & F Medical Products, 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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