BALL RECORDING ELECTRODE/STIMULATION PROBE— 510(k) K030517

Name: FDA 510(k) clearance K030517
Creator: U.S. Food and Drug Administration
Published: 2003-08-01

Substantially Equivalent

Viasys Healthcare, Inc.

FDA 510(k) clearance K030517 for BALL RECORDING ELECTRODE/STIMULATION PROBE, Substantially Equivalent on 2003-08-01. Applicant: Viasys Healthcare, Inc.. Device class: 2.

Clearance details

Applicant: Viasys Healthcare, Inc.
Product code: Code GZK
Device class: Class 2
Regulation: 21 CFR 882.1340
Advisory panel: Neurology
Date received: 2003-02-19
Decision date: 2003-08-01
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Stoughton, WI, US

Download summary PDF View on FDA.gov ↗

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