The following data is part of a premarket notification filed by Weaver & Co. with the FDA for Omniprep.
Device ID | K781989 |
510k Number | K781989 |
Device Name: | OMNIPREP |
Classification | Media, Electroconductive |
Applicant | WEAVER & CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | GYB |
CFR Regulation Number | 882.1275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-11-27 |
Decision Date | 1978-12-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OMNIPREP 90654050 not registered Live/Pending |
MAKE GREAT SALES LIMITED 2021-04-19 |
OMNIPREP 73276206 1177025 Dead/Cancelled |
White Consolidated Industries, Inc. 1980-09-02 |