NET-2000 MICROCURRENT STIMULATOR— 510(k) K060158

Name: FDA 510(k) clearance K060158
Creator: U.S. Food and Drug Administration
Published: 2006-10-13

Substantially Equivalent

Auri-Stem Medical, Inc.

FDA 510(k) clearance K060158 for NET-2000 MICROCURRENT STIMULATOR, Substantially Equivalent on 2006-10-13. Applicant: Auri-Stem Medical, Inc.. Device class: 2.

Clearance details

Applicant: Auri-Stem Medical, Inc.
Product code: Code QJQ
Device class: Class 2
Regulation: 21 CFR 882.5800
Advisory panel: Neurology
Date received: 2006-01-20
Decision date: 2006-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boulder, CO, US

Download summary PDF View on FDA.gov ↗

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