The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Digitron.
Device ID | K812721 |
510k Number | K812721 |
Device Name: | DIGITRON |
Classification | System, X-ray, Angiographic |
Applicant | SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | IZI |
CFR Regulation Number | 892.1600 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-09-28 |
Decision Date | 1981-11-04 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DIGITRON 79228584 5663540 Live/Registered |
Siemens Aktiengesellschaft 2018-01-02 |
DIGITRON 78755706 not registered Dead/Abandoned |
Digitron, Inc. 2005-11-17 |
DIGITRON 78478384 not registered Dead/Abandoned |
Digitron Electronic Corporation 2004-09-03 |
DIGITRON 77033760 3392455 Dead/Cancelled |
ANDA BRIDGE ENTERPRISE INC. 2006-10-31 |
DIGITRON 74198831 1725242 Dead/Cancelled |
JAVELINA CORPORATION, THE 1991-08-29 |
DIGITRON 73830665 not registered Dead/Abandoned |
DIGITRON AG 1989-10-11 |
DIGITRON 73773666 1633945 Dead/Cancelled |
DIGITRON AG 1989-01-09 |
DIGITRON 73589275 1424659 Dead/Cancelled |
SILTEC MARKETING INTERNATIONAL LTD. 1986-03-21 |
DIGITRON 73425045 1290792 Dead/Cancelled |
Javelina Corporation, The 1983-05-09 |
DIGITRON 73363055 1273411 Dead/Cancelled |
Siemens Gammasonics, Inc. 1982-05-28 |
DIGITRON 73324168 1230899 Dead/Cancelled |
Atlas Supply Company 1981-08-18 |
DIGITRON 73254726 1331750 Dead/Cancelled |
International Medical Corporation 1980-03-20 |