The following data is part of a premarket notification filed by Tomtec Imaging Systems, Gmbh with the FDA for 2d Cardiac Performance Analysis Mr 1.0.
Device ID | K120135 |
510k Number | K120135 |
Device Name: | 2D CARDIAC PERFORMANCE ANALYSIS MR 1.0 |
Classification | System, Image Processing, Radiological |
Applicant | TOMTEC IMAGING SYSTEMS, GMBH EDISONSTRASSE 6 Unterschleissheim, DE D-85716 |
Contact | Inge Scheidt |
Correspondent | Inge Scheidt 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 | 2012-01-17 |
Decision Date | 2012-04-13 |
Summary: | summary |