510(k) Report

FDA applicant

Essex Medical Systems Plus

Great Neck, NY1 decision2003–20030 recalls

FDA records 1 decision for Essex Medical Systems Plus (Great Neck, NY) in 2003: 1 510(k) clearance. All are in product code NFB (Conserver, Oxygen). 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 Essex Medical Systems Plus’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Essex Medical Systems Plus since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Essex Medical Systems Plus 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?

  • NFBConserver, Oxygen1decision

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.

  • K024023Essex High Pressure (HP) Ocd and Essex Escort Pneumatic ConserverEssex Medical Systems Plus · 20031cites it

What has FDA decided for it lately?

  • K024023Essex High Pressure (HP) Ocd and Essex Escort Pneumatic ConserverEssex Medical Systems Plus · 2003

The one decision as Essex Medical Systems Plus →

Other applicant names beginning “Essex”

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

Essex Cryogenics of Missouri, Inc. 5Essex Industries, Inc. 4Essex Industries, Inc. D/B/A Essex Cryogenics of M 1