The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc with the FDA for Scenium.
Device ID | K150192 |
510k Number | K150192 |
Device Name: | Scenium |
Classification | System, Image Processing, Radiological |
Applicant | SIEMENS MEDICAL SOLUTIONS USA, INC 810 INNOVATION DRIVE Knoxville, TN 37932 |
Contact | Alaine Medio |
Correspondent | Alaine Medio SIEMENS MEDICAL SOLUTIONS USA, INC 810 INNOVATION DRIVE Knoxville, TN 37932 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-01-28 |
Decision Date | 2015-03-29 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SCENIUM 88364502 not registered Live/Pending |
TECHNICOLOR 2019-03-31 |
SCENIUM 87816470 5584897 Live/Registered |
Siemens Medical Solutions USA, Inc. 2018-03-01 |
SCENIUM 86482753 5745716 Live/Registered |
RCA Trademark Management 2014-12-17 |
SCENIUM 85475410 4175121 Dead/Cancelled |
Montblanc-Simplo GmbH 2011-11-17 |
SCENIUM 85232506 not registered Dead/Abandoned |
TECHNICOLOR 2011-02-02 |
SCENIUM 79000803 2951880 Dead/Cancelled |
Montblanc-Simplo GmbH 2004-02-04 |
SCENIUM 78917298 3275008 Dead/Cancelled |
Siemens Molecular Imaging Limited 2006-06-26 |
SCENIUM 78657228 not registered Dead/Abandoned |
CTI Mirada Solutions Limited 2005-06-23 |
SCENIUM 76061072 2764716 Dead/Cancelled |
THOMSON INC. 2000-06-01 |