ELECTRO-GEL— 510(k) K111717

Substantially Equivalent

Electro-Cap Intl., Inc.

FDA 510(k) clearance K111717 for ELECTRO-GEL, Substantially Equivalent on 2012-01-05. Applicant: Electro-Cap Intl., Inc.. Device class: 2.

Clearance details

Applicant: Electro-Cap Intl., Inc.
Product code: Code GYB
Device class: Class 2
Regulation: 21 CFR 882.1275
Advisory panel: Neurology
Date received: 2011-06-20
Decision date: 2012-01-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eaton, OH, 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.