THE GALILEO VEGA-24 ELECTROENCEPHALOGRAPH— 510(k) K923950

Name: FDA 510(k) clearance K923950
Creator: U.S. Food and Drug Administration
Published: 1993-01-26

Substantially Equivalent

Biosound, Inc.

FDA 510(k) clearance K923950 for THE GALILEO VEGA-24 ELECTROENCEPHALOGRAPH, Substantially Equivalent on 1993-01-26. Applicant: Biosound, Inc.. Device class: 2.

Clearance details

Applicant: Biosound, Inc.
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1992-08-05
Decision date: 1993-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

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More clearances from Biosound, Inc.

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K963262 — ARTOSCAN M1997-03-28
K963662 — GALILEO EVOKED POTENTIALRE1997-02-26
K953716 — INTRACAVITY TRANSDUCERS1996-04-17

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