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 |