510(k) Report

FDA applicant

Woodson and Associates, LLC

Decatur, GA2 decisions1994–19980 recalls

FDA records 2 decisions for Woodson and Associates, LLC (Decatur, GA) from 1994 to 1998: 2 510(k) clearances. Most are in product codes KGI (Densitometer, Bone) and 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 Woodson and Associates, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Woodson and Associates, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Woodson and Associates, LLC 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?

  • KGIDensitometer, Bone1decision
  • KPSSystem, Tomography, Computed, Emission1decision

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.

  • K934040The OsteoreportWoodson and Associates, LLC · 19941cites it

What has FDA decided for it lately?

  • K981553Automated Medical Report WriterWoodson and Associates, LLC · 1998
  • K934040The OsteoreportWoodson and Associates, LLC · 1994

All 2 as Woodson and Associates, LLC →