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.

Lumiquick Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K130213 QUICKPROFILE SINGLE DRUG OF ABUSE DEVICE AND QUICK PROFILE MULTI-DRUGS OF ABUSE SCREEN DEVICELDJ2013-10-18 View
↑