FDA applicant

Viasys Neuro Care

Stoughton, WI2 decisions2006–20060 recalls

FDA records 2 decisions for Viasys Neuro Care (Stoughton, WI) in 2006: 2 510(k) clearances. Most are in product codes GWQ (Full-Montage Standard Electroencephalograph) and IYN (System, Imaging, Pulsed Doppler, Ultrasonic). Its devices cite 4 predicates, 0 of them its own earlier devices. 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 Viasys Neuro Care’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Viasys Neuro Care since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Viasys”

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

Viasys Healthcare GmbH 17 Viasys Medsystems 7 Viasys Respiratory Care, Inc. 3 Viasys Sleep Systems, LLC 1

Viasys Neuro Care

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Viasys”