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.

Orgentec Diagnostika GmbH

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K100499 ORGENTEC RHEUMATOID FACTOR EIADHR2010-10-27 View
510(k) K092399 ANTI-MUTATED CITRULLINATED VIMENTIN EIAOQZ2010-07-01 View
510(k) K030929 ANA DETECTLJM2003-05-02 View
↑