510(k) Report

FDA applicant

Renesco International, Inc.

Mchenry, IL4 decisions1979–19800 recalls

FDA records 4 decisions for Renesco International, Inc. (Mchenry, IL) from 1979 to 1980: 4 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and BZG (Spirometer, Diagnostic). 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 Renesco International, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Renesco International, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Renesco International, 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?

  • DPSElectrocardiograph3decisions
  • BZGSpirometer, Diagnostic1decision

What has FDA decided for it lately?

  • K800659Schiller MSG-1Renesco International, Inc. · 1980
  • K791422Minispirometer SP-1Renesco International, Inc. · 1979
  • K791421Miniscope MS-2B ElectrocardioscopeRenesco International, Inc. · 1979
  • K791420Minigraph MG-I ElectrocardiographRenesco International, Inc. · 1979

All 4 as Renesco International, Inc. →