FDA applicant

Neuro Vasx, Inc.

Plymouth, MN2 decisions1999–20010 recalls

FDA records 2 decisions for Neuro Vasx, Inc. (Plymouth, MN) from 1999 to 2001: 2 510(k) clearances. Most are in product codes DQO (Catheter, Intravascular, Diagnostic) and KRA (Catheter, Continuous Flush). Its devices cite 6 predicates, 1 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Neuro Vasx, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Neuro Vasx, 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 “Neuro”

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

Neuro Navigational Corp. 23 Neuro Supplies, Inc. 5 Neuro Technology 5 Neuro Kinetics, Inc. 4 Neuro Resource Group, Inc. 4 Neuro Therm, Inc. 3 Neuro Scan Labs 3 Neuro-Biometrix, Inc. 2 Neuro-Diagnostic Assoc. 2 Neuro Event Labs OY 1 Neuro-Fitness, LLC 1 Neuro Diagnostic Devices 1

Neuro Vasx, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Neuro”