510(k) Report

FDA applicant

Davicon, Inc.

Attleboro, MA2 decisions1992–19930 recalls

FDA records 2 decisions for Davicon, Inc. (Attleboro, MA) from 1992 to 1993: 2 510(k) clearances. All are in product code HCC (Device, Biofeedback). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Davicon, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Davicon, 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?

  • HCCDevice, Biofeedback2decisions

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.

  • K914920Biofeedback System/3Davicon, Inc. · 19922cite it
  • K914925Medac System/3Davicon, Inc. · 19931cites it

What has FDA decided for it lately?

  • K914925Medac System/3Davicon, Inc. · 1993
  • K914920Biofeedback System/3Davicon, Inc. · 1992

All 2 as Davicon, Inc. →