BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.— 510(k) K884852

Name: FDA 510(k) clearance K884852
Creator: U.S. Food and Drug Administration
Published: 1989-02-02

Substantially Equivalent

Moe

FDA 510(k) clearance K884852 for BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI., Substantially Equivalent on 1989-02-02. Applicant: Moe. Device class: 2.

Clearance details

Applicant: Moe
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1988-11-18
Decision date: 1989-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Soquel, CA, US

Download summary PDF View on FDA.gov ↗

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