K-number	K150402
Device name	Endoluminal Occlusion System-EOS
Applicant	Artventive Medical Group, Inc.
Product code	KRD
Device class	Class II
Decision date	Sep 25, 2015
Decision	Substantially Equivalent
Regulation	870.3300

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View the full FDA submission: accessdata.fda.gov

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Endoluminal Occlusion System-EOS

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