FDA 510(k), K133924, ENDOLUMINAL OCCLUSION SYSTEM (EOS)
FDA 510(k), K133924, ENDOLUMINAL OCCLUSION SYSTEM (EOS)
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510(K) Number: K133924
Device Name: ENDOLUMINAL OCCLUSION SYSTEM (EOS)
Manufacturer: ARTVENTIVE MEDICAL GROUP, INC
Device Classification Name: device, vascular, for promoting embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 12/23/2013
Decision Date: 12/03/2014
Regulation Medical Specialty: Cardiovascular
Device Name: ENDOLUMINAL OCCLUSION SYSTEM (EOS)
Manufacturer: ARTVENTIVE MEDICAL GROUP, INC
Device Classification Name: device, vascular, for promoting embolization
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 12/23/2013
Decision Date: 12/03/2014
Regulation Medical Specialty: Cardiovascular
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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