510(k) Report

FDA applicant

Eureduc

Antony, FR2 decisions1996–19960 recalls

FDA records 2 decisions for Eureduc (Antony, FR) in 1996: 2 510(k) clearances. All are in product code JOW (Sleeve, Limb, Compressible). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Eureduc since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Eureduc 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?

  • JOWSleeve, Limb, Compressible2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K954788Eureduc Pneumatic Drainage SystemEureduc · 1996
  • K960902Eureduc Pneumatic Drainage System Model TP03Eureduc · 1996

All 2 as Eureduc →