The following data is part of a premarket notification filed by Mid-america Medical Innovations, Llc. with the FDA for Cp Relief Wand.
Device ID | K133779 |
510k Number | K133779 |
Device Name: | CP RELIEF WAND |
Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Applicant | MID-AMERICA MEDICAL INNOVATIONS, LLC. 2704 INDUSTRIAL DRIVE Jefferson City, MO 65109 |
Contact | Norm Schroeder |
Correspondent | Norm Schroeder MID-AMERICA MEDICAL INNOVATIONS, LLC. 2704 INDUSTRIAL DRIVE Jefferson City, MO 65109 |
Product Code | GZJ |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-12-12 |
Decision Date | 2014-05-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CP RELIEF WAND 85923885 4626435 Live/Registered |
Mid-America Medical Innovations, LLC 2013-05-06 |