FDA applicant

The John Bunn Co.

Mchenry, IL20 decisions1976–19900 recalls

FDA records 20 decisions for The John Bunn Co. (Mchenry, IL) from 1976 to 1990: 20 510(k) clearances. Most are in product codes CAW (Generator, Oxygen, Portable) and CAP (Monitor, Airway Pressure (Includes Gauge…). 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 The John Bunn Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The John Bunn Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The John Bunn Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like The John Bunn Co.’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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Other applicant names beginning “The”

FDA records each applicant name separately; these may or may not be the same firm.

John O. Butler Co. 6 John F. Greer Co., Inc. 5 John Chatillon & Sons, Inc. 3 John Riccio 2 John Branch 1 John J. Navar, M.D. 1 John Caunt Scientific, Ltd. 1 John W. King 1 John Wagner Associates, Inc. 1 John J Riccio 1 John M. Rayhack 1 John Mfg., Ltd. 1

The John Bunn Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “The”