DISP. CONCENTRIC NEEDLE ELECTRODE (DCP-30, DCP-45)— 510(k) K896370

Name: FDA 510(k) clearance K896370
Creator: U.S. Food and Drug Administration
Published: 1989-12-22

Substantially Equivalent

Chalgren Enterprises, Inc.

FDA 510(k) clearance K896370 for DISP. CONCENTRIC NEEDLE ELECTRODE (DCP-30, DCP-45), Substantially Equivalent on 1989-12-22. Applicant: Chalgren Enterprises, Inc.. Device class: 2.

Clearance details

Applicant: Chalgren Enterprises, Inc.
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 1989-11-06
Decision date: 1989-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gilroy, CA, US

Download summary PDF View on FDA.gov ↗

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