ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000— 510(k) K863815

Name: FDA 510(k) clearance K863815
Creator: U.S. Food and Drug Administration
Published: 1987-06-02

Substantially Equivalent

Elcot, Inc.

FDA 510(k) clearance K863815 for ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000, Substantially Equivalent on 1987-06-02. Applicant: Elcot, Inc.. Device class: 2.

Clearance details

Applicant: Elcot, Inc.
Product code: Code QGH
Device class: Class 2
Regulation: 21 CFR 882.5940
Advisory panel: Neurology
Date received: 1986-09-30
Decision date: 1987-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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