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FDA 510(k) Applications Submitted by ARTVENTIVE MEDICAL GROUP, INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150402
02/18/2015
Endoluminal Occlusion System-EOS
ARTVENTIVE MEDICAL GROUP, INC
K133924
12/23/2013
ENDOLUMINAL OCCLUSION SYSTEM (EOS)
ARTVENTIVE MEDICAL GROUP, INC
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