FDA applicant

North American Philips Corp.

Mchenry, IL15 decisions1981–19840 recalls

FDA records 15 decisions for North American Philips Corp. (Mchenry, IL) from 1981 to 1984: 15 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and FLL (Continuous Measurement Thermometer). 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 North American Philips Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for North American Philips Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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North American Philips Corp.

Which product codes does it file in?

What has FDA decided for it lately?