510(k) Report

FDA applicant

Foregger Air Products & Chem., Inc.

Mchenry, IL3 decisions1976–19760 recalls

FDA records 3 decisions for Foregger Air Products & Chem., Inc. (Mchenry, IL) in 1976: 3 510(k) clearances. Most are in product codes CAH (Filter, Bacterial, Breathing-Circuit) and CAI (Circuit, Breathing (W Connector, Adaptor, Y…). 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 Foregger Air Products & Chem., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Foregger Air Products & Chem., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Foregger Air Products & Chem., 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 “Foregger”

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