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 |