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Somatex Medical Technologies GmbH

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K201863	Tumark Vision, Tumark Professional, Tumark Q, Tumark Professional Q-Shape	NEU	2021-02-18	View
510(k)	K182082	Tumark for Eviva, Tumark for Brevera	NEU	2018-10-31	View
510(k)	K180443	Tumark Vision	NEU	2018-03-22	View
510(k)	K111692	TUMARK FLEX FOR MAMMOTOME,TUMARK FLEX FOR ATEC	NEU	2011-11-08	View
510(k)	K102771	BIOPSY HANDY, MRI BIOPSY HANDY	KNW	2011-06-24	View
510(k)	K093064	TUMARK PROFESSIONAL, MODEL 271560, MR-TUMARK PROFESSIONAL, MODEL 601560	NEU	2010-02-17	View
510(k)	K073095	TUMARK PROFESSIONAL, MODEL 271560; MR- TUMARK PROFESSIONAL, MODEL 601560	NEU	2008-03-19	View

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