VIDEO EEG OPTION MODIFICATION— 510(k) K933951

Name: FDA 510(k) clearance K933951
Creator: U.S. Food and Drug Administration
Published: 1994-02-03

Substantially Equivalent

Esaote Biomedica Spa

FDA 510(k) clearance K933951 for VIDEO EEG OPTION MODIFICATION, Substantially Equivalent on 1994-02-03. Applicant: Esaote Biomedica Spa. Device class: 2.

Clearance details

Applicant: Esaote Biomedica Spa
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1993-08-12
Decision date: 1994-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, 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.