510(k) Report

FDA applicant

Proportional Technologies, Inc.

Houston, TX1 decision1997–19970 recalls

FDA records 1 decision for Proportional Technologies, Inc. (Houston, TX) in 1997: 1 510(k) clearance. All are in product code KPS (System, Tomography, Computed, Emission). 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, radiology panel, where it files most

How often FDA has decided Proportional Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Proportional Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Proportional 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?

  • KPSSystem, Tomography, Computed, Emission1decision

What has FDA decided for it lately?

  • K963730Protec (1024)Proportional Technologies, Inc. · 1997

The one decision as Proportional Technologies, Inc. →