510(k) Report

FDA applicant

Office of the Surgeon General, U.S. Army

Fort Detrick, MD1 decision2005–20050 recalls

FDA records 1 decision for Office of the Surgeon General, U.S. Army (Fort Detrick, MD) in 2005: 1 510(k) clearance. All are in product code NVQ (Bacteriophage And Controls, B. Anthracis Lysis). 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, microbiology panel, where it files most

How often FDA has decided Office of the Surgeon General, U.S. Army’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Office of the Surgeon General, U.S. Army since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Office of the Surgeon General, U.S. Army 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?

  • NVQBacteriophage And Controls, B. Anthracis Lysis1decision

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.

  • K051794Gamma Phage Lysis Assay for the Identification of Bacillus AnthracisOffice of the Surgeon General, U.S. Army · 20051cites it

What has FDA decided for it lately?

  • K051794Gamma Phage Lysis Assay for the Identification of Bacillus AnthracisOffice of the Surgeon General, U.S. Army · 2005

The one decision as Office of the Surgeon General, U.S. Army →