The following data is part of a premarket notification filed by Tomtec Imaging Systems Gmbh with the FDA for Tomtec-arena.
Device ID | K201632 |
510k Number | K201632 |
Device Name: | TOMTEC-ARENA |
Classification | System, Image Processing, Radiological |
Applicant | TOMTEC Imaging Systems GmbH Edisonstrasse 6 Unterschleissheim, DE 85716 |
Contact | Marc Bergenthal |
Correspondent | Marc Bergenthal TOMTEC Imaging Systems GmbH Edisonstrasse 6 Unterschleissheim, DE 85716 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-06-16 |
Decision Date | 2020-08-14 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
04260361440167 | K201632 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TOMTEC-ARENA 86004990 4566739 Live/Registered |
TomTec Imaging Systems GmbH 2013-07-09 |