# Phamatech

- Location (FDA's records): San Diego, CA
- FDA decisions: 62 (1996–2018): 62 510(k) clearances
- Names in FDA's records: Phamatech (47); Phamatech, Inc. (15)
- Product codes: MVO (14), DJG (6), DKZ (6), LCX (5), LCM (4), DIO (4), LAF (4), LDJ (3), JHI (3), DIS (3), CGJ (2), JXM (2)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 4 (2 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
- Drial Consultants, Inc.: 1 (https://510kreport.com/company/drial-consultants)

## Firms that cite its devices most
- Accu-Stat Diagnostics, Inc.: 1 (https://510kreport.com/company/accu-stat-diagnostics)
- Chemtron Biotech, Inc.: 1 (https://510kreport.com/company/chemtron-biotech)

## Its most-cited devices
- K070009: AT Home Drug Test Models, 9308T and 9308X (2007), cited by 2
- K003858: Modification to at Home Drug Test, Models 9150, 9068, and 9175 (2001), cited by 1
- K103295: Quickscreen Cocaine 150 Screening Test (2012), cited by 1

## Recent decisions
- K181945: QuickScreen Pro Multi Drug Screening Test, Model 9395Z (Oct 18, 2018)
- K131069: Quickscreen Amphetine 500 Test (May 14, 2014)
- K103295: Quickscreen Cocaine 150 Screening Test (Feb 1, 2012)
- K070009: AT Home Drug Test Models, 9308T and 9308X (Dec 7, 2007)
- K070098: Quickscreen Barbiturate 300 Screening Test, Models 9019, 9018; Multi Drug Screening Test, Model 9317T; Cup Multi Drug SC (Dec 7, 2007)
- K043599: Moments Menopause Check, Model 9113 (Feb 25, 2005)
- K043051: Quickscreen Oxycodone Test, Models 9120, 9120T, 9120X and 9121 (Feb 7, 2005)
- K043167: Phamatech Quickscreen Benzodiazepines Test, Models 9025, 9026, 9027T, 9153T and 9195X (Dec 29, 2004)

Source page: https://510kreport.com/company/phamatech