FDA applicant

Pharmaquest Corp.

Mchenry, IL14 decisions1981–19950 recalls

FDA records 14 decisions for Pharmaquest Corp. (Mchenry, IL) from 1981 to 1995: 14 510(k) clearances. Most are in product codes FOH (Mattress, Water, Temperature Regulated) and GYE (Encephalogram Telemetry System). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Pharmaquest Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Pharmaquest Corp.

Which product codes does it file in?

What has FDA decided for it lately?