510(k) Report

FDA applicant

Airmed Corp.

Mchenry, IL3 decisions1984–19840 recalls

FDA records 3 decisions for Airmed Corp. (Mchenry, IL) in 1984: 3 510(k) clearances. Most are in product codes FLL (Continuous Measurement Thermometer) and BZO (Set, Tubing And Support, Ventilator (W Harness)). 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 Airmed Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Airmed Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Airmed Corp.’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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