The following data is part of a premarket notification filed by Siemens Gammasonics, Inc. with the FDA for Litebox.
Device ID | K913252 |
510k Number | K913252 |
Device Name: | LITEBOX |
Classification | System, X-ray, Tomography, Computed |
Applicant | SIEMENS GAMMASONICS, INC. 2501 N. BARRINGTON RD. Hoffman Estates, IL 60195 -7372 |
Contact | Dennis W Henkelman |
Correspondent | Dennis W Henkelman SIEMENS GAMMASONICS, INC. 2501 N. BARRINGTON RD. Hoffman Estates, IL 60195 -7372 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-07-22 |
Decision Date | 1991-08-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LITEBOX 97498656 not registered Live/Pending |
Litebox USA LLC 2022-07-12 |
LITEBOX 87869305 not registered Dead/Abandoned |
LITEBOX 2018-04-09 |
LITEBOX 85158628 not registered Dead/Abandoned |
Universal Storage Containers LLC 2010-10-21 |
LITEBOX 78867236 not registered Dead/Abandoned |
Sorna Corporation 2006-04-21 |
LITEBOX 74024257 1710733 Dead/Cancelled |
Siemens Medical Systems, Inc. 1990-01-30 |
LITEBOX 73357052 1238190 Live/Registered |
Streamlight, Inc. 1982-03-29 |
LITEBOX 72427808 0976356 Dead/Expired |
BRUNSWICK ENGINEERING INC. 1972-06-20 |