FDA applicant

Airco/Ohio Medical Products

Mchenry, IL13 decisions1979–19840 recalls

FDA records 13 decisions for Airco/Ohio Medical Products (Mchenry, IL) from 1979 to 1984: 13 510(k) clearances. Most are in product codes BTR (Tube, Tracheal (W/Wo Connector)) and CBK (Ventilator, Continuous, Facility Use). 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 Airco/Ohio Medical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Airco/Ohio Medical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Airco/Ohio Medical Products by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Airco/Ohio Medical Products’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 “Airco/Ohio”

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

Airco, Inc. 3

Airco/Ohio Medical Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Airco/Ohio”