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.

Applied Dna Technologies, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K080467 BIONEXA SINGLE AND MULTI-STRIP CASSETTE/DIPSTICK DOA SCREEN PANELS ( AMP, BAR, BZO, COC, MET, MTD, MOR, PCP, TCA, THC,LDJ2008-11-25 View
510(k) K070921 BIONEXIA HCG PREGNANCY CASSETTE AND DIPSTICK TESTS, MODEL 08-HCG AND 02-HCGJHI2007-06-29 View
510(k) K071030 BIONEXIA HCG PREGNANCY SERUM/URINE CASSETTE AND DIPSTICK TESTS, MODELS 08-HCGC AND 02-HCGCJHI2007-06-29 View
510(k) K061005 ACCUSTEP DOA SINGLE AND MULTI-STRIP SCREEN PANELSDKZ2006-10-04 View
↑