RHYTHMLINK INTERNATIONAL SUBDERMAL NEEDLE ELECTRODES— 510(k) K022914

Name: FDA 510(k) clearance K022914
Creator: U.S. Food and Drug Administration
Published: 2002-12-20

Substantially Equivalent

Rhythmlink International, LLC

FDA 510(k) clearance K022914 for RHYTHMLINK INTERNATIONAL SUBDERMAL NEEDLE ELECTRODES, Substantially Equivalent on 2002-12-20. Applicant: Rhythmlink International, LLC. Device class: 2.

Clearance details

Applicant: Rhythmlink International, LLC
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 2002-09-03
Decision date: 2002-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cayce, SC, US

Download summary PDF View on FDA.gov ↗

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