EEG NEEDLE ELECTRODE— 510(k) K933796

Name: FDA 510(k) clearance K933796
Creator: U.S. Food and Drug Administration
Published: 1994-12-29

Substantially Equivalent

Cadwell Laboratories, Inc.

FDA 510(k) clearance K933796 for EEG NEEDLE ELECTRODE, Substantially Equivalent on 1994-12-29. Applicant: Cadwell Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Cadwell Laboratories, Inc.
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 1993-08-04
Decision date: 1994-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kennewick, WA, US

Download summary PDF View on FDA.gov ↗

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