510(k) Report

FDA applicant

Emergency Medical Techology

Irvine, CA1 decision2002–20020 recalls

FDA records 1 decision for Emergency Medical Techology (Irvine, CA) in 2002: 1 510(k) clearance. All are in product code BTL (Ventilator, Emergency, Powered (Resuscitator)). 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 Emergency Medical Techology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Emergency Medical Techology since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Emergency Medical Techology 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?

  • BTLVentilator, Emergency, Powered (Resuscitator)1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K021520Emt-CpapEmergency Medical Techology · 20022cite it

What has FDA decided for it lately?

  • K021520Emt-CpapEmergency Medical Techology · 2002

The one decision as Emergency Medical Techology →

Other applicant names beginning “Emergency”

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

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