FDA applicant

Bunnell Life Systems, Inc.

Mchenry, IL1 decision1981–19810 recalls

FDA records 1 decision for Bunnell Life Systems, Inc. (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code 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 Bunnell Life Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bunnell Life Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bunnell Life Systems, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Bunnell”

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

Bunnell, Inc. 1

Bunnell Life Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bunnell”