The following data is part of a premarket notification filed by Lorad Medical Systems, Inc. with the FDA for Lorad.
Device ID | K842102 |
510k Number | K842102 |
Device Name: | LORAD |
Classification | System, X-ray, Mammographic |
Applicant | LORAD MEDICAL SYSTEMS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | IZH |
CFR Regulation Number | 892.1710 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-05-25 |
Decision Date | 1984-07-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() LORAD 78094524 2733433 Live/Registered |
Jenving Technology AB 2001-11-21 |
![]() LORAD 74353391 1793517 Dead/Cancelled |
TREX MEDICAL CORPORATION 1993-01-28 |
![]() LORAD 74353089 1797697 Dead/Cancelled |
TREX MEDICAL CORPORATION 1993-01-27 |
![]() LORAD 74352775 1797695 Dead/Cancelled |
TREX MEDICAL CORPORATION 1993-01-27 |
![]() LORAD 74352771 1793513 Dead/Cancelled |
TREX MEDICAL CORPORATION 1993-01-27 |
![]() LORAD 73591133 1425641 Dead/Cancelled |
LORAD MEDICAL SYSTEMS, INC. 1986-04-01 |
![]() LORAD 73577024 1405623 Dead/Cancelled |
LEAR OPERATIONS RESEARCH & DEVELOPMENT CORP. 1986-01-09 |
![]() LORAD 72156382 0751284 Dead/Expired |
CORNING GLASS WORKS 1962-11-01 |