FDA applicant

Dept. of the Navy

Mchenry, IL1 decision1977–19770 recalls

FDA records 1 decision for Dept. of the Navy (Mchenry, IL) in 1977: 1 510(k) clearance. All are in product code 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 Dept. of the Navy’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dept. of the Navy since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Dept.”

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

Dept. of the Army 5

Dept. of the Navy

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dept.”