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

Vela Operations USA

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

Total Devices1
Categories1
Latest Approval2023-11-14
TypeNumberDevice NameCodeDate
510(k) K232092 Great Basin Toxigenic C. difficile Direct Test (CDF2) OZN 2023-11-14 View