ACTION POTENTIAL SIMULATION THERAPY DEVICE— 510(k) K955470

Name: FDA 510(k) clearance K955470
Creator: U.S. Food and Drug Administration
Published: 1996-10-22

Substantially Equivalent

Neurotech, Inc.

FDA 510(k) clearance K955470 for ACTION POTENTIAL SIMULATION THERAPY DEVICE, Substantially Equivalent on 1996-10-22. Applicant: Neurotech, Inc.. Device class: 2.

Clearance details

Applicant: Neurotech, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1995-11-30
Decision date: 1996-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tyler, 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.