BIOFEEDBACK ELECTROENCEPHALOGRAPH/ELECTROMYOGRAPH— 510(k) K894510

Name: FDA 510(k) clearance K894510
Creator: U.S. Food and Drug Administration
Published: 1990-01-16

Substantially Equivalent

Capscan Corp.

FDA 510(k) clearance K894510 for BIOFEEDBACK ELECTROENCEPHALOGRAPH/ELECTROMYOGRAPH, Substantially Equivalent on 1990-01-16. Applicant: Capscan Corp.. Device class: 2.

Clearance details

Applicant: Capscan Corp.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1989-07-19
Decision date: 1990-01-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ossining, NY, 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.