510(k) Report

FDA applicant

Williams Airway Intubator

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Williams Airway Intubator (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code CAE (Airway, Oropharyngeal, Anesthesiology). 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 Williams Airway Intubator’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Williams Airway Intubator since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • CAEAirway, Oropharyngeal, Anesthesiology1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K830767Williams Airway IntubatorWilliams Airway Intubator · 19831cites it

What has FDA decided for it lately?

  • K830767Williams Airway IntubatorWilliams Airway Intubator · 1983

The one decision as Williams Airway Intubator →

Other applicant names beginning “Williams”

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

Williams Gold Refining Co., Inc. 26Williams Medical Co. 5Williams Sound, LLC 4Williams Manufacturing Co. 4Williams Specialty Products, Inc. 2Williams Healthcare Systems, LLC 2Williams Dental Co., Inc. 2Williams Importing Company, Inc. 1Williams & Connolly 1Williams, the J.B. Co., Inc. 1