MEDELEC 2110 AND 2114 EEG— 510(k) K922548

Substantially Equivalent

Medelec Intl. Corp.

FDA 510(k) clearance K922548 for MEDELEC 2110 AND 2114 EEG, Substantially Equivalent on 1992-11-03. Applicant: Medelec Intl. Corp.. Device class: 2.

Clearance details

Applicant: Medelec Intl. Corp.
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1992-06-01
Decision date: 1992-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: England, GB

Download summary PDF View on FDA.gov ↗

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