The following data is part of a premarket notification filed by Siemens Medical Systems, Inc. with the FDA for Newcor.
Device ID | K020440 |
510k Number | K020440 |
Device Name: | NEWCOR |
Classification | Computer, Diagnostic, Programmable |
Applicant | SIEMENS MEDICAL SYSTEMS, INC. 186 WOOD AVENUE SOUTH Iselin, NJ 08830 |
Contact | Kathleen Rutherford |
Correspondent | Kathleen Rutherford SIEMENS MEDICAL SYSTEMS, INC. 186 WOOD AVENUE SOUTH Iselin, NJ 08830 |
Product Code | DQK |
CFR Regulation Number | 870.1425 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-02-11 |
Decision Date | 2002-12-03 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEWCOR 74243530 not registered Dead/Abandoned |
ORB ELECTRICAL STEELS LIMITED 1992-02-05 |
NEWCOR 73790835 1571592 Dead/Cancelled |
JMP-NEWCOR, INC. 1989-04-03 |
NEWCOR 73550569 1393800 Live/Registered |
NEWCOR, INC. 1985-07-29 |
NEWCOR 73494741 1372121 Dead/Cancelled |
BRITISH STEEL CORPORATION 1984-08-13 |
NEWCOR 73375514 not registered Dead/Abandoned |
NEWCOR INC. 1982-07-19 |
NEWCOR 73328665 1212468 Dead/Cancelled |
Newcor Inc. 1981-09-18 |