FDA applicant

Marquette Electronics, Inc.

Milwaukee, WI82 decisions1980–19971 recall

FDA records 82 decisions for Marquette Electronics, Inc. (Milwaukee, WI) from 1980 to 1997: 82 510(k) clearances. Most are in product codes DSI (Detector And Alarm, Arrhythmia) and DPS (Electrocardiograph). Its devices cite 9 predicates, 9 of them its own earlier devices. 1 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 Marquette Electronics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

1in 2013

2007high 1 (2013) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Marquette Electronics, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Marquette Electronics, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Marquette”

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

Marquette Medical, Inc. 17 Marquette Medical Systems, Inc. 9 Marquette Gas Analysis Corp. 2

Marquette Electronics, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Marquette”