EMG SYSTEM— 510(k) K111687

Substantially Equivalent

Myotronics-Noromed, Inc.

FDA 510(k) clearance K111687 for EMG SYSTEM, Substantially Equivalent on 2011-09-29. Applicant: Myotronics-Noromed, Inc.. Device class: 2.

Clearance details

Applicant: Myotronics-Noromed, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 2011-06-16
Decision date: 2011-09-29
Decision: Substantially Equivalent
Clearance type: Special
Location: Kent, WA, 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.