MINISTIM
Stimulator, Nerve, Transcutaneous, For Pain Relief
MEDICAL DESIGN & MANUFACTURING CORP.
The following data is part of a premarket notification filed by Medical Design & Manufacturing Corp. with the FDA for Ministim.
Pre-market Notification Details
| Device ID | K811224 |
| 510k Number | K811224 |
| Device Name: | MINISTIM |
| Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| Applicant | MEDICAL DESIGN & MANUFACTURING CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | GZJ |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-05-04 |
| Decision Date | 1981-06-02 |
Trademark Results [MINISTIM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MINISTIM 74270739 1784007 Live/Registered |
AVENT, INC. 1992-04-30 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.