THYMATRON 2000 ELECTROCONVULSIVE SYSTEM— 510(k) K945120

Name: FDA 510(k) clearance K945120
Creator: U.S. Food and Drug Administration
Published: 1995-10-26

Substantially Equivalent

Somatics, Inc.

FDA 510(k) clearance K945120 for THYMATRON 2000 ELECTROCONVULSIVE SYSTEM, Substantially Equivalent on 1995-10-26. Applicant: Somatics, Inc.. Device class: 2.

Clearance details

Applicant: Somatics, Inc.
Product code: Code QGH
Device class: Class 2
Regulation: 21 CFR 882.5940
Advisory panel: Neurology
Date received: 1994-10-19
Decision date: 1995-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Bluff, IL, US

Download summary PDF View on FDA.gov ↗

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