The following data is part of a premarket notification filed by Medical Design & Manufacturing Corp. with the FDA for Ministim.
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 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MINISTIM 74270739 1784007 Live/Registered |
AVENT, INC. 1992-04-30 |