510(k) Report

FDA applicant

Neuroscience Therapy Corp.

Kirkland, WA1 decision2006–20060 recalls

FDA records 1 decision for Neuroscience Therapy Corp. (Kirkland, WA) in 2006: 1 510(k) clearance. All are in product code BWK (Stimulator, Electro-Acupuncture). Its devices cite 1 predicate, 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

How often FDA has decided Neuroscience Therapy Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Neuroscience Therapy Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Neuroscience Therapy Corp.’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

Which product codes does it file in?

  • BWKStimulator, Electro-Acupuncture1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K050123P-Stim SystemNeuroscience Therapy Corp. · 20062cite it

What has FDA decided for it lately?

  • K050123P-Stim SystemNeuroscience Therapy Corp. · 2006

The one decision as Neuroscience Therapy Corp. →

Other applicant names beginning “Neuroscience”

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

Neuroscience, Inc. 4