CP RELIEF WAND— 510(k) K133779

Name: FDA 510(k) clearance K133779
Creator: U.S. Food and Drug Administration
Published: 2014-05-30

Substantially Equivalent

Mid-America Medical Innovations, LLC

FDA 510(k) clearance K133779 for CP RELIEF WAND, Substantially Equivalent on 2014-05-30. Applicant: Mid-America Medical Innovations, LLC. Device class: 2.

Clearance details

Applicant: Mid-America Medical Innovations, LLC
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2013-12-12
Decision date: 2014-05-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jefferson City, MO, US

Download summary PDF View on FDA.gov ↗

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