TECA MS-20 MYSTRO ELECTROPHYSIOLOGICAL— 510(k) K842886

Name: FDA 510(k) clearance K842886
Creator: U.S. Food and Drug Administration
Published: 1984-12-12

Substantially Equivalent

Teca, Inc.

FDA 510(k) clearance K842886 for TECA MS-20 MYSTRO ELECTROPHYSIOLOGICAL, Substantially Equivalent on 1984-12-12. Applicant: Teca, Inc.. Device class: 2.

Clearance details

Applicant: Teca, Inc.
Product code: Code GWN
Device class: Class 2
Regulation: 21 CFR 882.1460
Advisory panel: Neurology
Date received: 1984-07-23
Decision date: 1984-12-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasantiville, NY, US

Download summary PDF View on FDA.gov ↗

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