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.

Diagnosoft, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K111833 VIRTUELLZ2011-09-21 View
510(k) K100352 DIAGNOSOFT HARP MODEL 2.06LNH2010-03-11 View
510(k) K061368 DIAGNOSOFT HARPLNH2006-07-28 View
↑