The following data is part of a premarket notification filed by Tomtec Imaging Systems, Gmbh with the FDA for Tomtec-arena Tta2.
Device ID | K150122 |
510k Number | K150122 |
Device Name: | TOMTEC-ARENA TTA2 |
Classification | System, Image Processing, Radiological |
Applicant | TOMTEC IMAGING SYSTEMS, GMBH EDISONSTRASSE 6 Unterschleissheim, DE D-85716 |
Contact | Christine Klein |
Correspondent | Christine Klein TOMTEC IMAGING SYSTEMS, GMBH EDISONSTRASSE 6 Unterschleissheim, DE D-85716 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-01-20 |
Decision Date | 2015-02-13 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
04260361440143 | K150122 | 000 |