510(k) Report

FDA applicant

The Buddy Systems, Inc.

Northbrook, IL2 decisions1987–19870 recalls

FDA records 2 decisions for The Buddy Systems, Inc. (Northbrook, IL) in 1987: 2 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and DRX (Electrode, Electrocardiograph). 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 The Buddy Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Buddy Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Buddy Systems, 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?

  • DXNSystem, Measurement, Blood-Pressure, Non-Invasive1decision
  • DRXElectrode, Electrocardiograph1decision

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.

  • K864318The Buddy System/Health Information SystemThe Buddy Systems, Inc. · 19872cite it
  • K871748The Buddy System W/Optional Ecg ElectrodeThe Buddy Systems, Inc. · 19871cites it

What has FDA decided for it lately?

  • K871748The Buddy System W/Optional Ecg ElectrodeThe Buddy Systems, Inc. · 1987
  • K864318The Buddy System/Health Information SystemThe Buddy Systems, Inc. · 1987

All 2 as The Buddy Systems, Inc. →