NEUROMAPPER 1620— 510(k) K870263

Substantially Equivalent

Neuroscience, Inc.

FDA 510(k) clearance K870263 for NEUROMAPPER 1620, Substantially Equivalent on 1987-04-10. Applicant: Neuroscience, Inc.. Device class: 2.

Clearance details

Applicant: Neuroscience, Inc.
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1987-01-23
Decision date: 1987-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milpitas, CA, US

Download summary PDF View on FDA.gov ↗

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