FDA applicant

Electronic Monitors, Inc.

Euless, TX3 decisions1982–19930 recalls

FDA records 3 decisions for Electronic Monitors, Inc. (Euless, TX) from 1982 to 1993: 3 510(k) clearances. Most are in product codes GXY (Electrode, Cutaneous) and DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Electronic Monitors, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Electronic”

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

Electronic Waveform Laboratory, Inc. 6 Electronic Business Machine Co., Ltd. (Ebm) 3 Electronic Depilatory, Inc. 3 Electronic Diagnostics, Inc. 1 Electronic Medical Sciences, Inc. 1 Electronic Control Concepts 1 Electronic Waveform Lab, Inc. 1 Electronic Health Technologies, Inc. 1 Electronic Energy, Inc. 1 Electronic Monitoring Devices, Inc. 1

Electronic Monitors, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Electronic”