FDA applicant

Airco, Inc.

Virginia Beach, VA3 decisions1985–19860 recalls

FDA records 3 decisions for Airco, Inc. (Virginia Beach, VA) from 1985 to 1986: 3 510(k) clearances. Most are in product codes CAN (Regulator, Pressure, Gas Cylinder) and CAX (Flowmeter, Tube, Thorpe, Back-Pressure…). 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, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Airco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Airco, 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 “Airco”

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

Airco/Ohio Medical Products 13

Airco, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Airco”