EMG 3510/EMG 3510D MYOFEEDBACK MONITORS— 510(k) K810881

Name: FDA 510(k) clearance K810881
Creator: U.S. Food and Drug Administration
Published: 1981-05-27

Substantially Equivalent

Atlas Researches , Ltd.

FDA 510(k) clearance K810881 for EMG 3510/EMG 3510D MYOFEEDBACK MONITORS, Substantially Equivalent on 1981-05-27. Applicant: Atlas Researches , Ltd.. Device class: 2.

Clearance details

Applicant: Atlas Researches , Ltd.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1981-03-31
Decision date: 1981-05-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.