Applied Dna Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Applied Dna Technologies, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Applied Dna Technologies, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mission Viejo, US.
Historical record: 4 cleared submissions from 2006 to 2008. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Applied Dna Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Applied Dna Technologies, Inc.
4 devices
Cleared
Nov 25, 2008
BIONEXA SINGLE AND MULTI-STRIP CASSETTE/DIPSTICK DOA SCREEN PANELS ( AMP,...
Toxicology
278d
Cleared
Jun 29, 2007
BIONEXIA HCG PREGNANCY CASSETTE AND DIPSTICK TESTS, MODEL 08-HCG AND 02-HCG
Chemistry
88d
Cleared
Jun 29, 2007
BIONEXIA HCG PREGNANCY SERUM/URINE CASSETTE AND DIPSTICK TESTS, MODELS...
Chemistry
79d
Cleared
Oct 04, 2006
ACCUSTEP DOA SINGLE AND MULTI-STRIP SCREEN PANELS
Toxicology
176d