DISPOSABLE NEEDLE ELECTRODE (ALM), DISPOSABLE NEEDLE ELECTRODE (DLM)— 510(k) K974119

Name: FDA 510(k) clearance K974119
Creator: U.S. Food and Drug Administration
Published: 1998-01-28

Substantially Equivalent

Jack'S Electrodes

FDA 510(k) clearance K974119 for DISPOSABLE NEEDLE ELECTRODE (ALM), DISPOSABLE NEEDLE ELECTRODE (DLM), Substantially Equivalent on 1998-01-28. Applicant: Jack'S Electrodes. Device class: 2.

Clearance details

Applicant: Jack'S Electrodes
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 1997-10-31
Decision date: 1998-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Altadena, CA, US

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