K-number	K182082
Device name	Tumark for Eviva, Tumark for Brevera
Applicant	Somatex Medical Technologies GmbH
Product code	NEU
Device class	Class II
Decision date	Oct 31, 2018
Decision	Substantially Equivalent
Regulation	878.4300

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Source

View the full FDA submission: accessdata.fda.gov

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Tumark for Eviva, Tumark for Brevera

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