TD50 ELECTROMYOGRAPH— 510(k) K935017

Substantially Equivalent

Medelec Intl. Corp.

FDA 510(k) clearance K935017 for TD50 ELECTROMYOGRAPH, Substantially Equivalent on 1994-07-28. Applicant: Medelec Intl. Corp.. Device class: 2.

Clearance details

Applicant: Medelec Intl. Corp.
Product code: Code JXE
Device class: Class 2
Regulation: 21 CFR 882.1550
Advisory panel: Neurology
Date received: 1993-10-19
Decision date: 1994-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: England, GB

Download summary PDF View on FDA.gov ↗

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