510(k) Report

FDA applicant

Emergency Filtration Products, Inc.

Las Vegas, NV2 decisions1998–20020 recalls

FDA records 2 decisions for Emergency Filtration Products, Inc. (Las Vegas, NV) from 1998 to 2002: 2 510(k) clearances. Most are in product codes CAH (Filter, Bacterial, Breathing-Circuit) and CBP (Valve, Non-Rebreathing). 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 Filtration Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Emergency Filtration Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • CAHFilter, Bacterial, Breathing-Circuit1decision
  • CBPValve, Non-Rebreathing1decision

What has FDA decided for it lately?

  • K012958Breathing Circuit FilterEmergency Filtration Products, Inc. · 2002
  • K980052RespaideEmergency Filtration Products, Inc. · 1998

All 2 as Emergency Filtration Products, Inc. →

Other applicant names beginning “Emergency”

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

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