FDA applicant

Med Air Technology, Inc.

Springfield, MO3 decisions1986–19870 recalls

FDA records 3 decisions for Med Air Technology, Inc. (Springfield, MO) from 1986 to 1987: 3 510(k) clearances. Most are in product codes BYE (Attachment, Breathing, Positive End Expiratory…) and CBP (Valve, Non-Rebreathing). 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 Med Air Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med Air Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Med Air Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?