510(k) Report

FDA applicant

Fluid Propulsion Technologies, Inc.

Santa Clara, CA1 decision1997–19970 recalls

FDA records 1 decision for Fluid Propulsion Technologies, Inc. (Santa Clara, CA) in 1997: 1 510(k) clearance. 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 Fluid Propulsion Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fluid Propulsion Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fluid Propulsion Technologies, 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)1decision

Who builds on its devices?

Later devices cite its devices 3 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.

  • K970010FPT NebulizerFluid Propulsion Technologies, Inc. · 19973cite it

What has FDA decided for it lately?

  • K970010FPT NebulizerFluid Propulsion Technologies, Inc. · 1997

The one decision as Fluid Propulsion Technologies, Inc. →

Other applicant names beginning “Fluid”

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

Fluid Motion Biotechnologies, Inc. 1Fluid Process Systems, Inc. 1