Quantrx Biomedical Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Quantrx Biomedical Corporation - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Quantrx Biomedical Corporation has 4 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 4 cleared submissions from 2007 to 2009. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Quantrx Biomedical Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Quantrx Biomedical Corporation
4 devices
Cleared
Feb 11, 2009
RAPIDSENSE DRUGS OF ABUSE COCAINE (COC) 300 DEVICE, MODEL 900-0052
Toxicology
358d
Cleared
Jan 08, 2009
RAPIDSENSE DRUGS OF ABUSE PHENCYCLIDINE (PCP) 25 DEVICE WITH MODELS 900-0054
Toxicology
324d
Cleared
Dec 31, 2008
RAPIDSENSE DRUGS OF ABUSE METHAMPHETAMINE (MET) 1000 DEVICE, MODEL 900-0050
Toxicology
315d
Cleared
Oct 22, 2007
QUANTRX FEMALE FERTILITY TEST
Chemistry
244d