FDA applicant

Impulse Systems, Inc.

Madison, WI1 decision1989–19890 recalls

FDA records 1 decision for Impulse Systems, Inc. (Madison, WI) in 1989: 1 510(k) clearance. All are in product code JXE (Device, Nerve Conduction Velocity Measurement). 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 Impulse Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Impulse Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Impulse Systems, 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 “Impulse”

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

Impulse Dynamics (Usa), Inc. 1

Impulse Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Impulse”