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 |