# Quantrx Biomedical Corporation

- Location (FDA's records): San Diego, CA
- FDA decisions: 4 (2007–2009): 4 510(k) clearances
- Product codes: LAF (1), DIO (1), LCM (1), NGA (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- ACON Laboratories, Inc.: 4 (https://510kreport.com/company/acon-laboratories)
- Genosis, Ltd.: 1 (https://510kreport.com/company/genosis)
- Diagnostic Products Corp.: 1 (https://510kreport.com/company/diagnostic-products)

## Recent decisions
- K080436: Rapidsense Drugs of Abuse Cocaine (Coc) 300 Device, Model 900-0052 (Feb 11, 2009)
- K080431: Rapidsense Drugs of Abuse Phencyclidine (PCP) 25 Device with Models 900-0054 (Jan 8, 2009)
- K080455: Rapidsense  Drugs of Abuse Methamphetamine (Met) 1000 Device, Model 900-0050 (Dec 31, 2008)
- K070484: Quantrx Female Fertility Test (Oct 22, 2007)

Source page: https://510kreport.com/company/quantrx-biomedical