FDA 510(k) Applications Submitted by SOMATEX Medical Technologies GmbH
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K180443 |
02/20/2018 |
Tumark Vision |
SOMATEX Medical Technologies GmbH |
| K182082 |
08/02/2018 |
Tumark for Eviva, Tumark for Brevera |
Somatex Medical Technologies GmbH |
| K201863 |
07/06/2020 |
Tumark Vision, Tumark Professional, Tumark Q, Tumark Professional Q-Shape |
SOMATEX Medical Technologies GmbH |
| K111692 |
06/16/2011 |
TUMARK FLEX FOR MAMMOTOME,TUMARK FLEX FOR ATEC |
SOMATEX MEDICAL TECHNOLOGIES GMBH |
| K102771 |
09/24/2010 |
BIOPSY HANDY, MRI BIOPSY HANDY |
SOMATEX MEDICAL TECHNOLOGIES GMBH |
| K093064 |
09/30/2009 |
TUMARK PROFESSIONAL, MODEL 271560, MR-TUMARK PROFESSIONAL, MODEL 601560 |
SOMATEX MEDICAL TECHNOLOGIES GMBH |
| K073095 |
11/01/2007 |
TUMARK PROFESSIONAL, MODEL 271560; MR- TUMARK PROFESSIONAL, MODEL 601560 |
SOMATEX MEDICAL TECHNOLOGIES GMBH |
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