Muscle Stimulation System 110— 510(k) K150742

Name: FDA 510(k) clearance K150742
Creator: U.S. Food and Drug Administration
Published: 2015-07-23

Substantially Equivalent

Niveus Medical, Inc.

FDA 510(k) clearance K150742 for Muscle Stimulation System 110, Substantially Equivalent on 2015-07-23. Applicant: Niveus Medical, Inc.. Device class: 2.

Clearance details

Applicant: Niveus Medical, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2015-03-23
Decision date: 2015-07-23
Decision: Substantially Equivalent
Clearance type: Special
Location: Mountain View, CA, US

Download summary PDF View on FDA.gov ↗

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