EXTERNAL FUNCTIONAL NEUROMUSCULAR STIMULATOR— 510(k) K974514

Name: FDA 510(k) clearance K974514
Creator: U.S. Food and Drug Administration
Published: 1998-02-06

Substantially Equivalent

Neuromotion, Inc.

FDA 510(k) clearance K974514 for EXTERNAL FUNCTIONAL NEUROMUSCULAR STIMULATOR, Substantially Equivalent on 1998-02-06. Applicant: Neuromotion, Inc.. Device class: 2.

Clearance details

Applicant: Neuromotion, Inc.
Product code: Code GZI
Device class: Class 2
Regulation: 21 CFR 882.5810
Advisory panel: Neurology
Date received: 1997-12-01
Decision date: 1998-02-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Edmonton, Alberta, CA

Download summary PDF View on FDA.gov ↗

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