DISPOSIBLE EEG NEEDLE ELECTRODES— 510(k) K901280

Name: FDA 510(k) clearance K901280
Creator: U.S. Food and Drug Administration
Published: 1990-05-11

Substantially Equivalent

Medicotest, Inc.

FDA 510(k) clearance K901280 for DISPOSIBLE EEG NEEDLE ELECTRODES, Substantially Equivalent on 1990-05-11. Applicant: Medicotest, Inc.. Device class: 2.

Clearance details

Applicant: Medicotest, Inc.
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 1990-03-19
Decision date: 1990-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

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