510(k) Report

FDA applicant

Desco Industries, Inc.

Walnut, CA3 decisions1987–19870 recalls

FDA records 3 decisions for Desco Industries, Inc. (Walnut, CA) in 1987: 3 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and GZI (Stimulator, Neuromuscular, External Functional). 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 Desco Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Desco Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Desco Industries, 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?

  • DPSElectrocardiograph1decision
  • GZIStimulator, Neuromuscular, External Functional1decision
  • DSACable, Transducer And Electrode, Patient, (Including Connector)1decision

What has FDA decided for it lately?

  • K873492BSK-1033 Telemetry Monitoring CableDesco Industries, Inc. · 1987
  • K873608Tens LeadDesco Industries, Inc. · 1987
  • K870926C150-P Ecg CablesDesco Industries, Inc. · 1987

All 3 as Desco Industries, Inc. →