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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