The following data is part of a premarket notification filed by Tecnomed, Inc. with the FDA for Integron.
Device ID | K792327 |
510k Number | K792327 |
Device Name: | INTEGRON |
Classification | System, X-ray, Tomographic |
Applicant | TECNOMED, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | IZF |
CFR Regulation Number | 892.1740 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-11-19 |
Decision Date | 1979-12-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
INTEGRON 88059823 5697021 Live/Registered |
Terragene S.A. 2018-07-31 |
INTEGRON 79105954 4270257 Dead/Cancelled |
Braun GmbH 2011-09-21 |
INTEGRON 79067472 3761448 Dead/Cancelled |
INTEGRON B.V. 2008-08-13 |
INTEGRON 76298105 2585185 Live/Registered |
DGA Security Systems, Inc. 2001-08-13 |
INTEGRON 75268385 not registered Dead/Abandoned |
Ohio State University 1997-04-02 |
INTEGRON 75268297 not registered Dead/Abandoned |
Ohio State University, The 1997-04-02 |
INTEGRON 73823884 1595171 Dead/Cancelled |
BECTON, DICKINSON AND COMPANY 1989-09-07 |