VITOX
Supplement, Culture Media
OXOID U.S.A., INC.
The following data is part of a premarket notification filed by Oxoid U.s.a., Inc. with the FDA for Vitox.
Pre-market Notification Details
| Device ID | K810932 |
| 510k Number | K810932 |
| Device Name: | VITOX |
| Classification | Supplement, Culture Media |
| Applicant | OXOID U.S.A., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JSK |
| CFR Regulation Number | 866.2450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-04-06 |
| Decision Date | 1981-04-14 |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05032384011568 | K810932 | 000 |
Trademark Results [VITOX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VITOX 85136378 3950963 Live/Registered |
NSE Products, Inc. 2010-09-23 |
 VITOX 75586087 2307440 Dead/Cancelled |
Nu Skin International, Inc. 1998-11-10 |
 VITOX 74371530 not registered Dead/Abandoned |
Steal Guard Corporation 1993-03-24 |
 VITOX 74277865 not registered Dead/Abandoned |
Nu Skin International, Inc. 1992-05-21 |
 VITOX 73452308 1305723 Live/Registered |
BOC Group, Inc.; The 1983-11-09 |
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