BrainScope Ahead 100— 510(k) DEN140025

Unknown

Brainscope Company, Inc.

FDA 510(k) clearance DEN140025 for BrainScope Ahead 100, Unknown on 2014-11-17. Applicant: Brainscope Company, Inc.. Device class: 2.

Clearance details

Applicant: Brainscope Company, Inc.
Product code: Code PIW
Device class: Class 2
Regulation: 21 CFR 882.1450
Advisory panel: Neurology
Date received: 2014-08-20
Decision date: 2014-11-17
Decision: Unknown
Clearance type: Direct
Location: Bethesda, MD, US

View on FDA.gov ↗

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More clearances from Brainscope Company, Inc.

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Data sourced from openFDA. This site is unofficial and independent of the FDA.