FDA applicant

Honeywell, Inc.

Mchenry, IL69 decisions1976–19900 recalls

FDA records 69 decisions for Honeywell, Inc. (Mchenry, IL) from 1976 to 1990: 69 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). 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, cardiovascular panel, where it files most

How often FDA has decided Honeywell, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Honeywell, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Honeywell, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Honeywell”

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

Honeywell Hommed, LLC 8 Honeywell Safety Products 1

Honeywell, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Honeywell”