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.

American Diagnostica, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K080069 DIMERTESTDAP2008-02-13 View
510(k) K063323 SPECTROLYSE PAI-1, MODEL 101201GGP2007-08-15 View
510(k) K052124 ACTICLOT, MODEL 824GJS2005-10-17 View
510(k) K013637 ACTICHROME HEPARIN (ANTI-FIIA)KFF2002-04-16 View
510(k) K013492 IMUBIND TPA ELISA, MODEL 860GGP2002-03-13 View
510(k) K013318 ACTICHROME HEPARIN (ANTI-FXA), MODEL 832KFF2002-03-08 View
510(k) K013168 IMUBIND PLASMA PAI-1 ELISA,MODEL 822GGP2002-03-07 View
510(k) K012386 ACTICLOT PROTEIN S, MODEL 843LGGP2001-09-14 View
510(k) K940490 DV TEST AND DVV CONFIRMGIR1995-04-05 View
510(k) K935254 DVVTEST AND DVVCONFIRM LUPUS ANTICOAGULANT NORMAL AND ABNORMAL CONTROL PLASMAGIZ1994-09-19 View
↑