FDA applicant

Airway Products, Inc.

Blue Springs, MO1 decision1989–19890 recalls

FDA records 1 decision for Airway Products, Inc. (Blue Springs, MO) in 1989: 1 510(k) clearance. All are in product code 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 Airway Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Airway Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Airway Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Airway”

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

Airway Management, Inc. 6 Airway Technologies D/B/A Airway Management 1

Airway Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Airway”