Home › Brainscope Company, Inc. › Baseline Headset

Baseline Headset

Brainscope Company, Inc. · Model 99-1803-202 · UDI-DI 00852745007253

OLU PKQ PIW Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

A variant of the electrode headset that is to be used for Baseline sessions.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.