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 |