INTERX5000— 510(k) K042912

Substantially Equivalent

Neuro Resource Group, Inc.

FDA 510(k) clearance K042912 for INTERX5000, Substantially Equivalent on 2005-05-17. Applicant: Neuro Resource Group, Inc.. Device class: 2.

Clearance details

Applicant: Neuro Resource Group, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2004-10-21
Decision date: 2005-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irving, TX, 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.