CP RELIEF WAND

Stimulator, Nerve, Transcutaneous, For Pain Relief

MID-AMERICA MEDICAL INNOVATIONS, LLC.

The following data is part of a premarket notification filed by Mid-america Medical Innovations, Llc. with the FDA for Cp Relief Wand.

Pre-market Notification Details

Device IDK133779
510k NumberK133779
Device Name:CP RELIEF WAND
ClassificationStimulator, Nerve, Transcutaneous, For Pain Relief
Applicant MID-AMERICA MEDICAL INNOVATIONS, LLC. 2704 INDUSTRIAL DRIVE Jefferson City,  MO  65109
ContactNorm Schroeder
CorrespondentNorm Schroeder
MID-AMERICA MEDICAL INNOVATIONS, LLC. 2704 INDUSTRIAL DRIVE Jefferson City,  MO  65109
Product CodeGZJ  
CFR Regulation Number882.5890 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2013-12-12
Decision Date2014-05-30

Trademark Results [CP RELIEF WAND]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CP RELIEF WAND
CP RELIEF WAND
85923885 4626435 Live/Registered
Mid-America Medical Innovations, LLC
2013-05-06

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.