510(k) Report

FDA applicant

Ferraris Medical, Inc.

Washington, DC3 decisions1993–20000 recalls

FDA records 3 decisions for Ferraris Medical, Inc. (Washington, DC) from 1993 to 2000: 3 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and BZH (Meter, Peak Flow, Spirometry). 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 Ferraris Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ferraris Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ferraris Medical, Inc. 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
  • BZHMeter, Peak Flow, Spirometry1decision

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.

  • K992038PocketspacerFerraris Medical, Inc. · 19991cites it

What has FDA decided for it lately?

  • K993199Pocket Chamber Valved Aerosol Holding ChamberFerraris Medical, Inc. · 2000
  • K992038PocketspacerFerraris Medical, Inc. · 1999
  • K924343Wright Pocket Peak Flow MeterFerraris Medical, Inc. · 1993

All 3 as Ferraris Medical, Inc. →

Other applicant names beginning “Ferraris”

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

Ferraris Respiratory, Inc. 2