FDA applicant

U.S Army Medical Materiel Development Activity

Fort Detrick, MD2 decisions2011–20150 recalls

FDA records 2 decisions for U.S Army Medical Materiel Development Activity (Fort Detrick, MD) from 2011 to 2015: 2 510(k) clearances. Most are in product codes OQW (2009 H1n1 Influenza Virus (Swine Origin)…) and OCC (Respiratory Virus Panel Nucleic Acid Assay…). Its devices cite 3 predicates, 0 of them its own earlier devices. 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 U.S Army Medical Materiel Development Activity’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — U.S Army Medical Materiel Development Activity by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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U.S Army Medical Materiel Development Activity

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?