Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Genesis Digital Imaging, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K130374 OMNI-VUE 2 SYSTEMLLZ2013-08-29 View
510(k) K073062 OMNI-VUE SYSTEMLLZ2008-03-10 View
↑