The following data is part of a premarket notification filed by Inter-med/ Vista Dental Products with the FDA for V-mix.
Device ID | K193357 |
510k Number | K193357 |
Device Name: | V-Mix |
Classification | Cleanser, Root Canal |
Applicant | Inter-Med/ Vista Dental Products 2220 South Street Suite A Racine, WI 53404 |
Contact | Katherine Barry |
Correspondent | Katherine Barry Inter-Med/ Vista Dental Products 2220 South Street Suite A Racine, WI 53404 |
Product Code | KJJ |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-12-04 |
Decision Date | 2020-10-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
V-MIX 76340131 2835816 Dead/Cancelled |
Accentus plc 2001-11-20 |
V-MIX 75896971 2878128 Dead/Cancelled |
HOLIDAY ENTERTAINMENT CO., LTD. 2000-01-14 |