510(k) Report

FDA applicant

Project Marketing

Cary, NC2 decisions1998–20020 recalls

FDA records 2 decisions for Project Marketing (Cary, NC) from 1998 to 2002: 2 510(k) clearances. All are in product code CAF (Nebulizer (Direct Patient Interface)). 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 Project Marketing’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Project Marketing since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Project Marketing 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?

  • CAFNebulizer (Direct Patient Interface)2decisions

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.

  • K98007456 Series Aerosol GeneratorProject Marketing · 19981cites it
  • K02144356 Series Jet NebulizerProject Marketing · 20021cites it

What has FDA decided for it lately?

  • K02144356 Series Jet NebulizerProject Marketing · 2002
  • K98007456 Series Aerosol GeneratorProject Marketing · 1998

All 2 as Project Marketing →

Other applicant names beginning “Project”

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

Project Chemistry, Inc. 1