FDA applicant

Emergency Management Products, Inc.

Rockville, MD1 decision1985–19850 recalls

FDA records 1 decision for Emergency Management Products, Inc. (Rockville, MD) in 1985: 1 510(k) clearance. All are in product code KDQ (Bottle, Collection, Vacuum). 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, general hospital panel, where it files most

How often FDA has decided Emergency Management Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Emergency Management Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Emergency”

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

Emergency Filtration Products, Inc. 2 Emergency Situation Products 2 Emergency Medical Techology 1 Emergency Medical Supply, Inc. 1 Emergency Medical Devices, LLC 1 Emergency Medicine 1 Emergency Products and Research 1

Emergency Management Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Emergency”