The following data is part of a premarket notification filed by Vepro - Computersysteme Gmbh with the FDA for Medimage.
| Device ID | K972215 |
| 510k Number | K972215 |
| Device Name: | MEDIMAGE |
| Classification | System, Image Processing, Radiological |
| Applicant | VEPRO - COMPUTERSYSTEME GMBH AN DER TUCHBLEICHE 26 Pfungstadt, DE D-64319 |
| Contact | Harald G Roth |
| Correspondent | Harald G Roth VEPRO - COMPUTERSYSTEME GMBH AN DER TUCHBLEICHE 26 Pfungstadt, DE D-64319 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-06-13 |
| Decision Date | 1997-11-19 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEDIMAGE 74603161 2079660 Dead/Cancelled |
Vepro Computersysteme GmbH 1994-11-18 |
![]() MEDIMAGE 74139089 not registered Dead/Abandoned |
Medic Arts Graphics, Inc. 1991-02-14 |