510(k) Report

FDA applicant

Marshall Electronics, Inc.

Mchenry, IL3 decisions1978–19810 recalls

FDA records 3 decisions for Marshall Electronics, Inc. (Mchenry, IL) from 1978 to 1981: 3 510(k) clearances. Most are in product codes HGY (Pump, Breast, Non-Powered) and KME (Bedding, Disposable, Medical). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Marshall Electronics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Marshall Electronics, 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?

  • HGYPump, Breast, Non-Powered1decision
  • KMEBedding, Disposable, Medical1decision
  • LDEStethoscope, Manual1decision

What has FDA decided for it lately?

  • K813247Kaneson/Comfort Plus Manual Breast PumpMarshall Electronics, Inc. · 1981
  • K790411Auto Trauma KitMarshall Electronics, Inc. · 1979
  • K780023Black Bag, ElectronicMarshall Electronics, Inc. · 1978

All 3 as Marshall Electronics, Inc. →

Other applicant names beginning “Marshall”

FDA records each applicant name separately; these may or may not be the same firm.

Marshall Baby Products 2Marshall Levinson 1Marshall Davis, Inc. 1Marshall Latex Products Private, Ltd. 1