FDA applicant

Armstrong Ind., Inc.

Northbrook, IL5 decisions1982–19850 recalls

FDA records 5 decisions for Armstrong Ind., Inc. (Northbrook, IL) from 1982 to 1985: 5 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and CAE (Airway, Oropharyngeal, Anesthesiology). 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 Armstrong Ind., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Armstrong Ind., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Armstrong Ind., 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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Other applicant names beginning “Armstrong”

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

Armstrong Industries, Inc. 3 Armstrong Healthcare Limited 3 Armstrong Medical, Ltd. 1 Armstrong Industries, Inc. Dha Mediquip Int. Dha S 1

Armstrong Ind., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Armstrong”