FDA applicant
Neurocorp, Ltd.
FDA records 1 decision for Neurocorp, Ltd. (Tarrytown, NY) in 1998: 1 510(k) clearance. All are in product code GWQ (Full-Montage Standard Electroencephalograph). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Neurocorp, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Neurocorp, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Neurocorp, Ltd.’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