NEUROLINK IP, MODEL PK1113— 510(k) K081741

Name: FDA 510(k) clearance K081741
Creator: U.S. Food and Drug Administration
Published: 2008-10-31

Substantially Equivalent

Excel-Tech Ltd. (Xltek)

FDA 510(k) clearance K081741 for NEUROLINK IP, MODEL PK1113, Substantially Equivalent on 2008-10-31. Applicant: Excel-Tech Ltd. (Xltek). Device class: 2.

Clearance details

Applicant: Excel-Tech Ltd. (Xltek)
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 2008-06-19
Decision date: 2008-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oakville, CA

Download summary PDF View on FDA.gov ↗

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