510(k) Report

FDA applicant

B & F Medical Products, Inc.

Mchenry, IL18 decisions1976–19940 recalls

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, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

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.

FIG. 1 — B & F Medical Products, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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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